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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: 1-153535336-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=153535336&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 153535336,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_014624.4",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "NM_014624.4",
"protein_id": "NP_055439.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000368719.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014624.4"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000368719.9",
"protein_id": "ENSP00000357708.3",
"transcript_support_level": 1,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014624.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000368719.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "n.68G>T",
"hgvs_p": null,
"transcript": "ENST00000462951.2",
"protein_id": null,
"transcript_support_level": 1,
"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": "ENST00000462951.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000368720.6",
"protein_id": "ENSP00000357709.1",
"transcript_support_level": 3,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000368720.6"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000496817.5",
"protein_id": "ENSP00000473589.1",
"transcript_support_level": 2,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000496817.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896466.1",
"protein_id": "ENSP00000566525.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896466.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896467.1",
"protein_id": "ENSP00000566526.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896467.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896468.1",
"protein_id": "ENSP00000566527.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896468.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896469.1",
"protein_id": "ENSP00000566528.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896469.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896470.1",
"protein_id": "ENSP00000566529.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896470.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896471.1",
"protein_id": "ENSP00000566530.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896471.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896472.1",
"protein_id": "ENSP00000566531.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896472.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896473.1",
"protein_id": "ENSP00000566532.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896473.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000925440.1",
"protein_id": "ENSP00000595499.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925440.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000925441.1",
"protein_id": "ENSP00000595500.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925441.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000925442.1",
"protein_id": "ENSP00000595501.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925442.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000925443.1",
"protein_id": "ENSP00000595502.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925443.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896474.1",
"protein_id": "ENSP00000566533.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 89,
"cds_start": 4,
"cds_end": null,
"cds_length": 270,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896474.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000954696.1",
"protein_id": "ENSP00000624755.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 89,
"cds_start": 4,
"cds_end": null,
"cds_length": 270,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954696.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000896475.1",
"protein_id": "ENSP00000566534.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 87,
"cds_start": 4,
"cds_end": null,
"cds_length": 264,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896475.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "ENST00000462776.2",
"protein_id": "ENSP00000473547.1",
"transcript_support_level": 2,
"aa_start": 2,
"aa_end": null,
"aa_length": 84,
"cds_start": 4,
"cds_end": null,
"cds_length": 255,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000462776.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser",
"transcript": "XM_017002033.2",
"protein_id": "XP_016857522.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 90,
"cds_start": 4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017002033.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
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},
{
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],
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{
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},
{
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},
{
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],
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{
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},
{
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"consequences": [
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],
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"gene_symbol": "ENSG00000238279",
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"transcript": "ENST00000420695.4",
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},
{
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],
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"gene_symbol": "ENSG00000238279",
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"transcript": "ENST00000819290.1",
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},
{
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"protein_coding": false,
"strand": true,
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"downstream_gene_variant"
],
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"exon_count": 3,
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"gene_symbol": "ENSG00000238279",
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"biotype": "pseudogene",
"feature": "ENST00000819291.1"
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],
"gene_symbol": "S100A6",
"gene_hgnc_id": 10496,
"dbsnp": "rs147817499",
"frequency_reference_population": 0.000012392618,
"hom_count_reference_population": 0,
"allele_count_reference_population": 20,
"gnomad_exomes_af": 0.0000129988,
"gnomad_genomes_af": 0.00000657073,
"gnomad_exomes_ac": 19,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.06778153777122498,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.41999998688697815,
"splice_prediction_selected": "Uncertain_significance",
"splice_source_selected": "max_spliceai",
"revel_score": 0.046,
"revel_prediction": "Benign",
"alphamissense_score": 0.0835,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.67,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.1,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.42,
"spliceai_max_prediction": "Uncertain_significance",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_014624.4",
"gene_symbol": "S100A6",
"hgnc_id": 10496,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.4G>T",
"hgvs_p": "p.Ala2Ser"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "XR_007066630.1",
"gene_symbol": "LOC124904423",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.913C>A",
"hgvs_p": null
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000819283.1",
"gene_symbol": "ENSG00000238279",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.555+238C>A",
"hgvs_p": null
}
],
"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
}