← 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: 1-61725045-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=61725045&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 61725045,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_032027.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "NM_032027.3",
"protein_id": "NP_114416.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 207,
"cds_start": 76,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000606498.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_032027.3"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000606498.5",
"protein_id": "ENSP00000475700.1",
"transcript_support_level": 5,
"aa_start": 26,
"aa_end": null,
"aa_length": 207,
"cds_start": 76,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_032027.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000606498.5"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000371180.7",
"protein_id": "ENSP00000360222.2",
"transcript_support_level": 5,
"aa_start": 26,
"aa_end": null,
"aa_length": 207,
"cds_start": 76,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000371180.7"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000371177.2",
"protein_id": "ENSP00000475297.1",
"transcript_support_level": 5,
"aa_start": 26,
"aa_end": null,
"aa_length": 186,
"cds_start": 76,
"cds_end": null,
"cds_length": 561,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000371177.2"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000964149.1",
"protein_id": "ENSP00000634208.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 268,
"cds_start": 76,
"cds_end": null,
"cds_length": 807,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964149.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000855760.1",
"protein_id": "ENSP00000525819.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 262,
"cds_start": 76,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855760.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000922032.1",
"protein_id": "ENSP00000592091.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 242,
"cds_start": 76,
"cds_end": null,
"cds_length": 729,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000922032.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000855758.1",
"protein_id": "ENSP00000525817.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 207,
"cds_start": 76,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855758.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000922031.1",
"protein_id": "ENSP00000592090.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 207,
"cds_start": 76,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000922031.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000964150.1",
"protein_id": "ENSP00000634209.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 207,
"cds_start": 76,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964150.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000964148.1",
"protein_id": "ENSP00000634207.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 205,
"cds_start": 76,
"cds_end": null,
"cds_length": 618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964148.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000855759.1",
"protein_id": "ENSP00000525818.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 202,
"cds_start": 76,
"cds_end": null,
"cds_length": 609,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855759.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000922030.1",
"protein_id": "ENSP00000592089.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 140,
"cds_start": 76,
"cds_end": null,
"cds_length": 423,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000922030.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "ENST00000855761.1",
"protein_id": "ENSP00000525820.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 109,
"cds_start": 76,
"cds_end": null,
"cds_length": 330,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855761.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "XM_047431743.1",
"protein_id": "XP_047287699.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 277,
"cds_start": 76,
"cds_end": null,
"cds_length": 834,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431743.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "XM_047431744.1",
"protein_id": "XP_047287700.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 262,
"cds_start": 76,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431744.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu",
"transcript": "XM_047431745.1",
"protein_id": "XP_047287701.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 262,
"cds_start": 76,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431745.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.76G>C",
"hgvs_p": null,
"transcript": "ENST00000371178.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000371178.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.22G>C",
"hgvs_p": null,
"transcript": "ENST00000468586.5",
"protein_id": "ENSP00000475186.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000468586.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.67G>C",
"hgvs_p": null,
"transcript": "ENST00000488206.5",
"protein_id": "ENSP00000476178.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000488206.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.4G>C",
"hgvs_p": null,
"transcript": "ENST00000494926.5",
"protein_id": "ENSP00000475844.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000494926.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.76G>C",
"hgvs_p": null,
"transcript": "ENST00000496465.1",
"protein_id": "ENSP00000475529.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000496465.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.97G>C",
"hgvs_p": null,
"transcript": "NR_135160.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_135160.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.97G>C",
"hgvs_p": null,
"transcript": "NR_135161.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_135161.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.97G>C",
"hgvs_p": null,
"transcript": "NR_135162.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_135162.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"hgvs_c": "n.97G>C",
"hgvs_p": null,
"transcript": "XR_007064044.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_007064044.1"
}
],
"gene_symbol": "TM2D1",
"gene_hgnc_id": 24142,
"dbsnp": "rs200877661",
"frequency_reference_population": 0.0001264047,
"hom_count_reference_population": 0,
"allele_count_reference_population": 204,
"gnomad_exomes_af": 0.000123834,
"gnomad_genomes_af": 0.000151089,
"gnomad_exomes_ac": 181,
"gnomad_genomes_ac": 23,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.012125462293624878,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.032,
"revel_prediction": "Benign",
"alphamissense_score": 0.0777,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.48,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.19,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_032027.3",
"gene_symbol": "TM2D1",
"hgnc_id": 24142,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.76G>C",
"hgvs_p": "p.Val26Leu"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}