← Back to variant description
GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 9-105604218-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=105604218&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 16,
"criteria": [
"BP6_Very_Strong",
"BA1"
],
"effects": [
"missense_variant"
],
"gene_symbol": "FKTN",
"hgnc_id": 3622,
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"inheritance_mode": "AR,AD",
"pathogenic_score": 0,
"score": -16,
"transcript": "NM_006731.2",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP6_Very_Strong,BA1",
"acmg_score": -16,
"allele_count_reference_population": 21863,
"alphamissense_prediction": null,
"alphamissense_score": 0.0736,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.18,
"chr": "9",
"clinvar_classification": "Benign/Likely benign",
"clinvar_disease": " 4, type A,Cardiovascular phenotype,Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies),Walker-Warburg congenital muscular dystrophy,not provided,not specified",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2 B:8",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.002128303050994873,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7455,
"cdna_start": 588,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "NM_001079802.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000357998.10",
"protein_coding": true,
"protein_id": "NP_001073270.1",
"strand": true,
"transcript": "NM_001079802.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 7455,
"cdna_start": 588,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000357998.10",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001079802.2",
"protein_coding": true,
"protein_id": "ENSP00000350687.6",
"strand": true,
"transcript": "ENST00000357998.10",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7364,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000223528.6",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000223528.2",
"strand": true,
"transcript": "ENST00000223528.6",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 7036,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000602526.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*411G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000473347.1",
"strand": true,
"transcript": "ENST00000602526.1",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2876,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000602661.6",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.491G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000473540.2",
"strand": true,
"transcript": "ENST00000602661.6",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 7036,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000602526.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*411G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000473347.1",
"strand": true,
"transcript": "ENST00000602526.1",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 489,
"aa_ref": "G",
"aa_start": 153,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2908,
"cdna_start": 938,
"cds_end": null,
"cds_length": 1470,
"cds_start": 457,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000922141.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.457G>A",
"hgvs_p": "p.Gly153Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000592200.1",
"strand": true,
"transcript": "ENST00000922141.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7590,
"cdna_start": 723,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "NM_001351496.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338425.1",
"strand": true,
"transcript": "NM_001351496.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7364,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NM_006731.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_006722.2",
"strand": true,
"transcript": "NM_006731.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3862,
"cdna_start": 839,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000906332.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576391.1",
"strand": true,
"transcript": "ENST00000906332.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2667,
"cdna_start": 734,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "ENST00000906335.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576394.1",
"strand": true,
"transcript": "ENST00000906335.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2828,
"cdna_start": 1515,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000906336.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576395.1",
"strand": true,
"transcript": "ENST00000906336.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2217,
"cdna_start": 904,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000906337.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576396.1",
"strand": true,
"transcript": "ENST00000906337.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7440,
"cdna_start": 576,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000922138.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000592197.1",
"strand": true,
"transcript": "ENST00000922138.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6459,
"cdna_start": 657,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "ENST00000922139.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000592198.1",
"strand": true,
"transcript": "ENST00000922139.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6651,
"cdna_start": 851,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000922140.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000592199.1",
"strand": true,
"transcript": "ENST00000922140.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7644,
"cdna_start": 777,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "ENST00000922142.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000592201.1",
"strand": true,
"transcript": "ENST00000922142.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4548,
"cdna_start": 806,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000967515.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000637574.1",
"strand": true,
"transcript": "ENST00000967515.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 460,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2427,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1383,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000906334.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576393.1",
"strand": true,
"transcript": "ENST00000906334.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 450,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3045,
"cdna_start": 399,
"cds_end": null,
"cds_length": 1353,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000676310.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000501585.1",
"strand": true,
"transcript": "ENST00000676310.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 448,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2019,
"cdna_start": 401,
"cds_end": null,
"cds_length": 1347,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000674633.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000502164.1",
"strand": true,
"transcript": "ENST00000674633.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 438,
"aa_ref": "G",
"aa_start": 102,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7688,
"cdna_start": 821,
"cds_end": null,
"cds_length": 1317,
"cds_start": 304,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_001351497.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Gly102Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338426.1",
"strand": true,
"transcript": "NM_001351497.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 430,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2503,
"cdna_start": 588,
"cds_end": null,
"cds_length": 1293,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "NM_001198963.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001185892.1",
"strand": true,
"transcript": "NM_001198963.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 430,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1700,
"cdna_start": 587,
"cds_end": null,
"cds_length": 1293,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000448551.6",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000399140.2",
"strand": true,
"transcript": "ENST00000448551.6",
"transcript_support_level": 2
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 412,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7394,
"cdna_start": 496,
"cds_end": null,
"cds_length": 1239,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NM_001351498.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338427.1",
"strand": true,
"transcript": "NM_001351498.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 405,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4284,
"cdna_start": 723,
"cds_end": null,
"cds_length": 1218,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "ENST00000675668.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000502113.1",
"strand": true,
"transcript": "ENST00000675668.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 373,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2419,
"cdna_start": 494,
"cds_end": null,
"cds_length": 1122,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000906333.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576392.1",
"strand": true,
"transcript": "ENST00000906333.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 373,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7181,
"cdna_start": 578,
"cds_end": null,
"cds_length": 1122,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000922137.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000592196.1",
"strand": true,
"transcript": "ENST00000922137.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1845,
"cdna_start": 724,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_011518368.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011516670.1",
"strand": true,
"transcript": "XM_011518368.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1710,
"cdna_start": 589,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_011518369.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011516671.1",
"strand": true,
"transcript": "XM_011518369.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1791,
"cdna_start": 670,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_011518373.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011516675.1",
"strand": true,
"transcript": "XM_011518373.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1618,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_011518374.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011516676.1",
"strand": true,
"transcript": "XM_011518374.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1992,
"cdna_start": 871,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "XM_017014462.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016869951.1",
"strand": true,
"transcript": "XM_017014462.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1857,
"cdna_start": 736,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422967.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278923.1",
"strand": true,
"transcript": "XM_047422967.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1955,
"cdna_start": 834,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422968.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278924.1",
"strand": true,
"transcript": "XM_047422968.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1938,
"cdna_start": 817,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "XM_047422969.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278925.1",
"strand": true,
"transcript": "XM_047422969.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 488,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2215,
"cdna_start": 1094,
"cds_end": null,
"cds_length": 1467,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422970.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278926.1",
"strand": true,
"transcript": "XM_047422970.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 472,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7806,
"cdna_start": 736,
"cds_end": null,
"cds_length": 1419,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422971.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278927.1",
"strand": true,
"transcript": "XM_047422971.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 472,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7567,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1419,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_047422972.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278928.1",
"strand": true,
"transcript": "XM_047422972.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 465,
"aa_ref": "G",
"aa_start": 102,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1508,
"cdna_start": 383,
"cds_end": null,
"cds_length": 1398,
"cds_start": 304,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_011518379.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Gly102Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011516681.1",
"strand": true,
"transcript": "XM_011518379.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7701,
"cdna_start": 834,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422973.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278929.1",
"strand": true,
"transcript": "XM_047422973.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7738,
"cdna_start": 871,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "XM_047422974.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278930.1",
"strand": true,
"transcript": "XM_047422974.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7603,
"cdna_start": 736,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422975.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278931.1",
"strand": true,
"transcript": "XM_047422975.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7836,
"cdna_start": 969,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422976.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278932.1",
"strand": true,
"transcript": "XM_047422976.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7537,
"cdna_start": 670,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422977.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278933.1",
"strand": true,
"transcript": "XM_047422977.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7684,
"cdna_start": 817,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "XM_047422978.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278934.1",
"strand": true,
"transcript": "XM_047422978.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8108,
"cdna_start": 1241,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "XM_047422979.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278935.1",
"strand": true,
"transcript": "XM_047422979.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 461,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7782,
"cdna_start": 915,
"cds_end": null,
"cds_length": 1386,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422980.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278936.1",
"strand": true,
"transcript": "XM_047422980.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 438,
"aa_ref": "G",
"aa_start": 102,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8595,
"cdna_start": 1728,
"cds_end": null,
"cds_length": 1317,
"cds_start": 304,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "XM_047422981.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.304G>A",
"hgvs_p": "p.Gly102Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278937.1",
"strand": true,
"transcript": "XM_047422981.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 426,
"aa_ref": "G",
"aa_start": 63,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3368,
"cdna_start": 2246,
"cds_end": null,
"cds_length": 1281,
"cds_start": 187,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "XM_047422982.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.187G>A",
"hgvs_p": "p.Gly63Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278938.1",
"strand": true,
"transcript": "XM_047422982.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 426,
"aa_ref": "G",
"aa_start": 63,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3897,
"cdna_start": 2775,
"cds_end": null,
"cds_length": 1281,
"cds_start": 187,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "XM_047422983.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.187G>A",
"hgvs_p": "p.Gly63Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278939.1",
"strand": true,
"transcript": "XM_047422983.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 412,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7487,
"cdna_start": 589,
"cds_end": null,
"cds_length": 1239,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422984.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278940.1",
"strand": true,
"transcript": "XM_047422984.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 412,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7622,
"cdna_start": 724,
"cds_end": null,
"cds_length": 1239,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422985.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278941.1",
"strand": true,
"transcript": "XM_047422985.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 412,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7634,
"cdna_start": 736,
"cds_end": null,
"cds_length": 1239,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422986.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278942.1",
"strand": true,
"transcript": "XM_047422986.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 412,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7568,
"cdna_start": 670,
"cds_end": null,
"cds_length": 1239,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422987.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278943.1",
"strand": true,
"transcript": "XM_047422987.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 400,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1360,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1203,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_017014475.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016869964.1",
"strand": true,
"transcript": "XM_017014475.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 396,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1695,
"cdna_start": 724,
"cds_end": null,
"cds_length": 1191,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422988.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278944.1",
"strand": true,
"transcript": "XM_047422988.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 396,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1560,
"cdna_start": 589,
"cds_end": null,
"cds_length": 1191,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422989.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278945.1",
"strand": true,
"transcript": "XM_047422989.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 384,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7303,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1155,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_047422990.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278946.1",
"strand": true,
"transcript": "XM_047422990.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 373,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7192,
"cdna_start": 589,
"cds_end": null,
"cds_length": 1122,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422991.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278947.1",
"strand": true,
"transcript": "XM_047422991.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 373,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8735,
"cdna_start": 2132,
"cds_end": null,
"cds_length": 1122,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422992.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278948.1",
"strand": true,
"transcript": "XM_047422992.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 373,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7100,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1122,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_047422993.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278949.1",
"strand": true,
"transcript": "XM_047422993.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 370,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1643,
"cdna_start": 724,
"cds_end": null,
"cds_length": 1113,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422994.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278950.1",
"strand": true,
"transcript": "XM_047422994.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 370,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1508,
"cdna_start": 589,
"cds_end": null,
"cds_length": 1113,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422995.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278951.1",
"strand": true,
"transcript": "XM_047422995.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 370,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1655,
"cdna_start": 736,
"cds_end": null,
"cds_length": 1113,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422996.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278952.1",
"strand": true,
"transcript": "XM_047422996.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 370,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1416,
"cdna_start": 497,
"cds_end": null,
"cds_length": 1113,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_047422997.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278953.1",
"strand": true,
"transcript": "XM_047422997.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6972,
"cdna_start": 497,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_006717014.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006717077.1",
"strand": true,
"transcript": "XM_006717014.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7199,
"cdna_start": 724,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_011518391.3",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011516693.1",
"strand": true,
"transcript": "XM_011518391.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7064,
"cdna_start": 589,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047422998.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278954.1",
"strand": true,
"transcript": "XM_047422998.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7211,
"cdna_start": 736,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047422999.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278955.1",
"strand": true,
"transcript": "XM_047422999.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7309,
"cdna_start": 834,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_047423000.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278956.1",
"strand": true,
"transcript": "XM_047423000.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7145,
"cdna_start": 670,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047423001.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278957.1",
"strand": true,
"transcript": "XM_047423001.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 271,
"aa_ref": "G",
"aa_start": 125,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7390,
"cdna_start": 915,
"cds_end": null,
"cds_length": 816,
"cds_start": 373,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_047423002.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Gly125Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278958.1",
"strand": true,
"transcript": "XM_047423002.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 329,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7708,
"cdna_start": null,
"cds_end": null,
"cds_length": 990,
"cds_start": null,
"consequences": [
"5_prime_UTR_variant"
],
"exon_count": 13,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_001351499.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.-24G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338428.1",
"strand": true,
"transcript": "NM_001351499.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 329,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7573,
"cdna_start": null,
"cds_end": null,
"cds_length": 990,
"cds_start": null,
"consequences": [
"5_prime_UTR_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "NM_001351500.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.-24G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338429.1",
"strand": true,
"transcript": "NM_001351500.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 329,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7481,
"cdna_start": null,
"cds_end": null,
"cds_length": 990,
"cds_start": null,
"consequences": [
"5_prime_UTR_variant"
],
"exon_count": 11,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "NM_001351501.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.-24G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338430.1",
"strand": true,
"transcript": "NM_001351501.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 329,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7801,
"cdna_start": null,
"cds_end": null,
"cds_length": 990,
"cds_start": null,
"consequences": [
"5_prime_UTR_variant"
],
"exon_count": 14,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_001351502.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "c.-24G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001338431.1",
"strand": true,
"transcript": "NM_001351502.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 786,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 6,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000374705.5",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*300G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000363837.5",
"strand": true,
"transcript": "ENST00000374705.5",
"transcript_support_level": 5
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1930,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000642177.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.373G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000495864.1",
"strand": true,
"transcript": "ENST00000642177.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2134,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 15,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000642537.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*235G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000495945.1",
"strand": true,
"transcript": "ENST00000642537.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1579,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 10,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000642644.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*496G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000494674.1",
"strand": true,
"transcript": "ENST00000642644.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2233,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000642952.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*371G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000493886.1",
"strand": true,
"transcript": "ENST00000642952.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2016,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000645933.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*371G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000495852.1",
"strand": true,
"transcript": "ENST00000645933.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3564,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 12,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000674563.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.373G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502153.1",
"strand": true,
"transcript": "ENST00000674563.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3291,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 9,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000675232.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*508G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502043.1",
"strand": true,
"transcript": "ENST00000675232.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2412,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 7,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000675443.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.491G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502643.1",
"strand": true,
"transcript": "ENST00000675443.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 7226,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 10,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000675695.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.373G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502460.1",
"strand": true,
"transcript": "ENST00000675695.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 7897,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000675736.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.491G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502809.1",
"strand": true,
"transcript": "ENST00000675736.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 7504,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 9,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000676011.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.1540G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "ENST00000676011.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3125,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 7,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000676192.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*293G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502158.1",
"strand": true,
"transcript": "ENST00000676192.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1349,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 9,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000676371.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*180G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000501556.1",
"strand": true,
"transcript": "ENST00000676371.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 7363,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 10,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "NR_147213.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.588G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_147213.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 7535,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 11,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NR_147214.2",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.496G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_147214.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 786,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 6,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000374705.5",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*300G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000363837.5",
"strand": true,
"transcript": "ENST00000374705.5",
"transcript_support_level": 5
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2134,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 15,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000642537.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*235G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000495945.1",
"strand": true,
"transcript": "ENST00000642537.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1579,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 10,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000642644.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*496G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000494674.1",
"strand": true,
"transcript": "ENST00000642644.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2233,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 13,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000642952.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*371G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000493886.1",
"strand": true,
"transcript": "ENST00000642952.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2016,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 14,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000645933.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*371G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000495852.1",
"strand": true,
"transcript": "ENST00000645933.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3291,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 9,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000675232.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*508G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502043.1",
"strand": true,
"transcript": "ENST00000675232.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3125,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 7,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000676192.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*293G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502158.1",
"strand": true,
"transcript": "ENST00000676192.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1349,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 9,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000676371.1",
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"hgvs_c": "n.*180G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000501556.1",
"strand": true,
"transcript": "ENST00000676371.1",
"transcript_support_level": null
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs34006675",
"effect": "missense_variant",
"frequency_reference_population": 0.013560939,
"gene_hgnc_id": 3622,
"gene_symbol": "FKTN",
"gnomad_exomes_ac": 17068,
"gnomad_exomes_af": 0.0116907,
"gnomad_exomes_homalt": 224,
"gnomad_genomes_ac": 4795,
"gnomad_genomes_af": 0.0314963,
"gnomad_genomes_homalt": 165,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 389,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Benign/Likely benign",
"phenotype_combined": "Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4|not specified|Walker-Warburg congenital muscular dystrophy|Cardiovascular phenotype|not provided",
"phylop100way_prediction": "Benign",
"phylop100way_score": 1.684,
"pos": 105604218,
"ref": "G",
"revel_prediction": "Benign",
"revel_score": 0.245,
"splice_prediction_selected": "Uncertain_significance",
"splice_score_selected": 0.20999999344348907,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Uncertain_significance",
"spliceai_max_score": 0.21,
"transcript": "NM_006731.2"
}
]
}