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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: 7-74063224-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=74063224&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 74063224,
"ref": "G",
"alt": "C",
"effect": "missense_variant,splice_region_variant",
"transcript": "ENST00000252034.12",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1858G>C",
"hgvs_p": "p.Gly620Arg",
"transcript": "NM_000501.4",
"protein_id": "NP_000492.2",
"transcript_support_level": null,
"aa_start": 620,
"aa_end": null,
"aa_length": 724,
"cds_start": 1858,
"cds_end": null,
"cds_length": 2175,
"cdna_start": 1873,
"cdna_end": null,
"cdna_length": 3397,
"mane_select": "ENST00000252034.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1858G>C",
"hgvs_p": "p.Gly620Arg",
"transcript": "ENST00000252034.12",
"protein_id": "ENSP00000252034.7",
"transcript_support_level": 1,
"aa_start": 620,
"aa_end": null,
"aa_length": 724,
"cds_start": 1858,
"cds_end": null,
"cds_length": 2175,
"cdna_start": 1873,
"cdna_end": null,
"cdna_length": 3397,
"mane_select": "NM_000501.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1876G>C",
"hgvs_p": "p.Gly626Arg",
"transcript": "ENST00000380562.8",
"protein_id": "ENSP00000369936.4",
"transcript_support_level": 1,
"aa_start": 626,
"aa_end": null,
"aa_length": 730,
"cds_start": 1876,
"cds_end": null,
"cds_length": 2193,
"cdna_start": 1923,
"cdna_end": null,
"cdna_length": 2240,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1828G>C",
"hgvs_p": "p.Gly610Arg",
"transcript": "ENST00000458204.5",
"protein_id": "ENSP00000403162.1",
"transcript_support_level": 1,
"aa_start": 610,
"aa_end": null,
"aa_length": 714,
"cds_start": 1828,
"cds_end": null,
"cds_length": 2145,
"cdna_start": 1853,
"cdna_end": null,
"cdna_length": 3147,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1873G>C",
"hgvs_p": "p.Gly625Arg",
"transcript": "ENST00000357036.9",
"protein_id": "ENSP00000349540.5",
"transcript_support_level": 1,
"aa_start": 625,
"aa_end": null,
"aa_length": 711,
"cds_start": 1873,
"cds_end": null,
"cds_length": 2136,
"cdna_start": 1891,
"cdna_end": null,
"cdna_length": 3361,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1801G>C",
"hgvs_p": "p.Gly601Arg",
"transcript": "ENST00000380576.9",
"protein_id": "ENSP00000369950.5",
"transcript_support_level": 1,
"aa_start": 601,
"aa_end": null,
"aa_length": 705,
"cds_start": 1801,
"cds_end": null,
"cds_length": 2118,
"cdna_start": 1814,
"cdna_end": null,
"cdna_length": 3109,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1771G>C",
"hgvs_p": "p.Gly591Arg",
"transcript": "ENST00000380575.8",
"protein_id": "ENSP00000369949.4",
"transcript_support_level": 1,
"aa_start": 591,
"aa_end": null,
"aa_length": 677,
"cds_start": 1771,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 1802,
"cdna_end": null,
"cdna_length": 3043,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1714G>C",
"hgvs_p": "p.Gly572Arg",
"transcript": "ENST00000380584.8",
"protein_id": "ENSP00000369958.4",
"transcript_support_level": 1,
"aa_start": 572,
"aa_end": null,
"aa_length": 658,
"cds_start": 1714,
"cds_end": null,
"cds_length": 1977,
"cdna_start": 1744,
"cdna_end": null,
"cdna_length": 3214,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.2044G>C",
"hgvs_p": "p.Gly682Arg",
"transcript": "NM_001278939.2",
"protein_id": "NP_001265868.1",
"transcript_support_level": null,
"aa_start": 682,
"aa_end": null,
"aa_length": 786,
"cds_start": 2044,
"cds_end": null,
"cds_length": 2361,
"cdna_start": 2059,
"cdna_end": null,
"cdna_length": 3583,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.2044G>C",
"hgvs_p": "p.Gly682Arg",
"transcript": "ENST00000692049.1",
"protein_id": "ENSP00000510104.1",
"transcript_support_level": null,
"aa_start": 682,
"aa_end": null,
"aa_length": 786,
"cds_start": 2044,
"cds_end": null,
"cds_length": 2361,
"cdna_start": 2044,
"cdna_end": null,
"cdna_length": 2361,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1957G>C",
"hgvs_p": "p.Gly653Arg",
"transcript": "ENST00000320399.10",
"protein_id": "ENSP00000313565.6",
"transcript_support_level": 5,
"aa_start": 653,
"aa_end": null,
"aa_length": 757,
"cds_start": 1957,
"cds_end": null,
"cds_length": 2274,
"cdna_start": 1957,
"cdna_end": null,
"cdna_length": 2274,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1876G>C",
"hgvs_p": "p.Gly626Arg",
"transcript": "NM_001278915.2",
"protein_id": "NP_001265844.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 730,
"cds_start": 1876,
"cds_end": null,
"cds_length": 2193,
"cdna_start": 1891,
"cdna_end": null,
"cdna_length": 3415,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1828G>C",
"hgvs_p": "p.Gly610Arg",
"transcript": "NM_001278917.2",
"protein_id": "NP_001265846.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 714,
"cds_start": 1828,
"cds_end": null,
"cds_length": 2145,
"cdna_start": 1843,
"cdna_end": null,
"cdna_length": 3367,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1873G>C",
"hgvs_p": "p.Gly625Arg",
"transcript": "NM_001081754.3",
"protein_id": "NP_001075223.1",
"transcript_support_level": null,
"aa_start": 625,
"aa_end": null,
"aa_length": 711,
"cds_start": 1873,
"cds_end": null,
"cds_length": 2136,
"cdna_start": 1888,
"cdna_end": null,
"cdna_length": 3358,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1858G>C",
"hgvs_p": "p.Gly620Arg",
"transcript": "NM_001278912.2",
"protein_id": "NP_001265841.1",
"transcript_support_level": null,
"aa_start": 620,
"aa_end": null,
"aa_length": 706,
"cds_start": 1858,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 1873,
"cdna_end": null,
"cdna_length": 3343,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1858G>C",
"hgvs_p": "p.Gly620Arg",
"transcript": "ENST00000445912.5",
"protein_id": "ENSP00000389857.1",
"transcript_support_level": 2,
"aa_start": 620,
"aa_end": null,
"aa_length": 706,
"cds_start": 1858,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 2257,
"cdna_end": null,
"cdna_length": 2583,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1801G>C",
"hgvs_p": "p.Gly601Arg",
"transcript": "NM_001081755.3",
"protein_id": "NP_001075224.1",
"transcript_support_level": null,
"aa_start": 601,
"aa_end": null,
"aa_length": 705,
"cds_start": 1801,
"cds_end": null,
"cds_length": 2118,
"cdna_start": 1816,
"cdna_end": null,
"cdna_length": 3340,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1786G>C",
"hgvs_p": "p.Gly596Arg",
"transcript": "NM_001278914.2",
"protein_id": "NP_001265843.1",
"transcript_support_level": null,
"aa_start": 596,
"aa_end": null,
"aa_length": 700,
"cds_start": 1786,
"cds_end": null,
"cds_length": 2103,
"cdna_start": 1801,
"cdna_end": null,
"cdna_length": 3325,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1786G>C",
"hgvs_p": "p.Gly596Arg",
"transcript": "ENST00000414324.5",
"protein_id": "ENSP00000392575.1",
"transcript_support_level": 2,
"aa_start": 596,
"aa_end": null,
"aa_length": 700,
"cds_start": 1786,
"cds_end": null,
"cds_length": 2103,
"cdna_start": 1845,
"cdna_end": null,
"cdna_length": 3139,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1816G>C",
"hgvs_p": "p.Gly606Arg",
"transcript": "NM_001081753.3",
"protein_id": "NP_001075222.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 692,
"cds_start": 1816,
"cds_end": null,
"cds_length": 2079,
"cdna_start": 1831,
"cdna_end": null,
"cdna_length": 3301,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1816G>C",
"hgvs_p": "p.Gly606Arg",
"transcript": "ENST00000429192.5",
"protein_id": "ENSP00000391129.1",
"transcript_support_level": 2,
"aa_start": 606,
"aa_end": null,
"aa_length": 692,
"cds_start": 1816,
"cds_end": null,
"cds_length": 2079,
"cdna_start": 1831,
"cdna_end": null,
"cdna_length": 3298,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELN",
"gene_hgnc_id": 3327,
"hgvs_c": "c.1771G>C",
"hgvs_p": "p.Gly591Arg",
"transcript": "NM_001081752.3",
"protein_id": "NP_001075221.1",
"transcript_support_level": null,
"aa_start": 591,
"aa_end": null,
"aa_length": 677,
"cds_start": 1771,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 1786,
"cdna_end": null,
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},
{
"aa_ref": "G",
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"protein_coding": true,
"strand": true,
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"missense_variant",
"splice_region_variant"
],
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"exon_count": 30,
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"gene_symbol": "ELN",
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"hgvs_c": "c.1723G>C",
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"transcript": "XM_047419979.1",
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},
{
"aa_ref": "G",
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"protein_coding": true,
"strand": true,
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"missense_variant",
"splice_region_variant"
],
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"gene_symbol": "ELN",
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"hgvs_c": "c.1717G>C",
"hgvs_p": "p.Gly573Arg",
"transcript": "XM_047419980.1",
"protein_id": "XP_047275936.1",
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"aa_start": 573,
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"cds_start": 1717,
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"cdna_start": 1732,
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"mane_plus": null,
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"feature": null
}
],
"gene_symbol": "ELN",
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"dbsnp": "rs727503034",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.6510019302368164,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.7120000123977661,
"splice_prediction_selected": "Benign",
"splice_source_selected": "dbscSNV1_RF",
"revel_score": 0.155,
"revel_prediction": "Benign",
"alphamissense_score": 0.7568,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.22,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.369,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.57,
"spliceai_max_prediction": "Pathogenic",
"dbscsnv_ada_score": 0.992378323842916,
"dbscsnv_ada_prediction": "Pathogenic",
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 3,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3",
"acmg_by_gene": [
{
"score": 3,
"benign_score": 0,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000252034.12",
"gene_symbol": "ELN",
"hgnc_id": 3327,
"effects": [
"missense_variant",
"splice_region_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1858G>C",
"hgvs_p": "p.Gly620Arg"
}
],
"clinvar_disease": "Supravalvar aortic stenosis",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Supravalvar aortic stenosis",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}