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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: 14-100342508-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=100342508&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 100342508,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "ENST00000392882.7",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "NM_004184.4",
"protein_id": "NP_004175.2",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1141,
"cdna_end": null,
"cdna_length": 2639,
"mane_select": "ENST00000392882.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "ENST00000392882.7",
"protein_id": "ENSP00000376620.2",
"transcript_support_level": 1,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1141,
"cdna_end": null,
"cdna_length": 2639,
"mane_select": "NM_004184.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "ENST00000355338.6",
"protein_id": "ENSP00000347495.2",
"transcript_support_level": 1,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1622,
"cdna_end": null,
"cdna_length": 3092,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "ENST00000557135.5",
"protein_id": "ENSP00000451460.1",
"transcript_support_level": 1,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1271,
"cdna_end": null,
"cdna_length": 2080,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "NM_173701.2",
"protein_id": "NP_776049.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1144,
"cdna_end": null,
"cdna_length": 2642,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.880C>T",
"hgvs_p": "p.Leu294Leu",
"transcript": "NM_213645.2",
"protein_id": "NP_998810.1",
"transcript_support_level": null,
"aa_start": 294,
"aa_end": null,
"aa_length": 430,
"cds_start": 880,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 972,
"cdna_end": null,
"cdna_length": 2470,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.880C>T",
"hgvs_p": "p.Leu294Leu",
"transcript": "NM_213646.2",
"protein_id": "NP_998811.1",
"transcript_support_level": null,
"aa_start": 294,
"aa_end": null,
"aa_length": 430,
"cds_start": 880,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 969,
"cdna_end": null,
"cdna_length": 2467,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.880C>T",
"hgvs_p": "p.Leu294Leu",
"transcript": "ENST00000344102.9",
"protein_id": "ENSP00000339485.5",
"transcript_support_level": 5,
"aa_start": 294,
"aa_end": null,
"aa_length": 430,
"cds_start": 880,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 1230,
"cdna_end": null,
"cdna_length": 2690,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.880C>T",
"hgvs_p": "p.Leu294Leu",
"transcript": "ENST00000358655.8",
"protein_id": "ENSP00000351481.4",
"transcript_support_level": 2,
"aa_start": 294,
"aa_end": null,
"aa_length": 430,
"cds_start": 880,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 980,
"cdna_end": null,
"cdna_length": 2466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.880C>T",
"hgvs_p": "p.Leu294Leu",
"transcript": "ENST00000556645.5",
"protein_id": "ENSP00000451887.1",
"transcript_support_level": 5,
"aa_start": 294,
"aa_end": null,
"aa_length": 430,
"cds_start": 880,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 1713,
"cdna_end": null,
"cdna_length": 2508,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.259C>T",
"hgvs_p": "p.Leu87Leu",
"transcript": "ENST00000554601.1",
"protein_id": "ENSP00000451891.1",
"transcript_support_level": 2,
"aa_start": 87,
"aa_end": null,
"aa_length": 184,
"cds_start": 259,
"cds_end": null,
"cds_length": 555,
"cdna_start": 261,
"cdna_end": null,
"cdna_length": 719,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_017021627.3",
"protein_id": "XP_016877116.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1268,
"cdna_end": null,
"cdna_length": 2766,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_024449707.2",
"protein_id": "XP_024305475.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1229,
"cdna_end": null,
"cdna_length": 2727,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431757.1",
"protein_id": "XP_047287713.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1304,
"cdna_end": null,
"cdna_length": 2802,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431758.1",
"protein_id": "XP_047287714.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1180,
"cdna_end": null,
"cdna_length": 2678,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431759.1",
"protein_id": "XP_047287715.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1353,
"cdna_end": null,
"cdna_length": 2851,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431760.1",
"protein_id": "XP_047287716.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1250,
"cdna_end": null,
"cdna_length": 2748,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431761.1",
"protein_id": "XP_047287717.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1271,
"cdna_end": null,
"cdna_length": 2769,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431762.1",
"protein_id": "XP_047287718.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1253,
"cdna_end": null,
"cdna_length": 2751,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431763.1",
"protein_id": "XP_047287719.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1274,
"cdna_end": null,
"cdna_length": 2772,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu",
"transcript": "XM_047431764.1",
"protein_id": "XP_047287720.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 471,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1256,
"cdna_end": null,
"cdna_length": 2754,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.964C>T",
"hgvs_p": "p.Leu322Leu",
"transcript": "XM_047431765.1",
"protein_id": "XP_047287721.1",
"transcript_support_level": null,
"aa_start": 322,
"aa_end": null,
"aa_length": 458,
"cds_start": 964,
"cds_end": null,
"cds_length": 1377,
"cdna_start": 1084,
"cdna_end": null,
"cdna_length": 2582,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"hgvs_c": "c.880C>T",
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"aa_start": 294,
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"aa_length": 430,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
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"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
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"exon_count": 6,
"intron_rank": null,
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"gene_symbol": "WARS1",
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"hgvs_c": "n.1015C>T",
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"transcript": "ENST00000554950.1",
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"cds_start": -4,
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},
{
"aa_ref": null,
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"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
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"exon_count": 2,
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"gene_symbol": "WARS1",
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"cdna_length": 499,
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},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 2,
"intron_rank": 1,
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"gene_symbol": "ENSG00000258666",
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"hgvs_c": "n.114+8605G>A",
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"transcript": "ENST00000557226.1",
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"cds_start": -4,
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"cdna_length": 385,
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"biotype": null,
"feature": null
}
],
"gene_symbol": "WARS1",
"gene_hgnc_id": 12729,
"dbsnp": "rs9453",
"frequency_reference_population": 0.7346516,
"hom_count_reference_population": 438903,
"allele_count_reference_population": 1185378,
"gnomad_exomes_af": 0.73989,
"gnomad_genomes_af": 0.684258,
"gnomad_exomes_ac": 1081416,
"gnomad_genomes_ac": 103962,
"gnomad_exomes_homalt": 402139,
"gnomad_genomes_homalt": 36764,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.4399999976158142,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.25999999046325684,
"splice_prediction_selected": "Uncertain_significance",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.44,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 4.085,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.26,
"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": -16,
"acmg_classification": "Benign",
"acmg_criteria": "BP6_Very_Strong,BA1",
"acmg_by_gene": [
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP6_Very_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000392882.7",
"gene_symbol": "WARS1",
"hgnc_id": 12729,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.1003C>T",
"hgvs_p": "p.Leu335Leu"
},
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP6_Very_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000557226.1",
"gene_symbol": "ENSG00000258666",
"hgnc_id": 58289,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.114+8605G>A",
"hgvs_p": null
}
],
"clinvar_disease": " distal hereditary motor, type 9,Neuronopathy,WARS1-related disorder,not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:3",
"phenotype_combined": "not provided|Neuronopathy, distal hereditary motor, type 9|WARS1-related disorder",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}