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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: 8-28110384-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=28110384&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "8",
"pos": 28110384,
"ref": "A",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_018091.6",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "NM_018091.6",
"protein_id": "NP_060561.3",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 547,
"cds_start": 408,
"cds_end": null,
"cds_length": 1644,
"cdna_start": 484,
"cdna_end": null,
"cdna_length": 3148,
"mane_select": "ENST00000256398.13",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_018091.6"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "ENST00000256398.13",
"protein_id": "ENSP00000256398.8",
"transcript_support_level": 1,
"aa_start": 136,
"aa_end": null,
"aa_length": 547,
"cds_start": 408,
"cds_end": null,
"cds_length": 1644,
"cdna_start": 484,
"cdna_end": null,
"cdna_length": 3148,
"mane_select": "NM_018091.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000256398.13"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.366A>C",
"hgvs_p": "p.Arg122Ser",
"transcript": "ENST00000521015.5",
"protein_id": "ENSP00000428449.1",
"transcript_support_level": 1,
"aa_start": 122,
"aa_end": null,
"aa_length": 533,
"cds_start": 366,
"cds_end": null,
"cds_length": 1602,
"cdna_start": 491,
"cdna_end": null,
"cdna_length": 3158,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000521015.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "ENST00000900018.1",
"protein_id": "ENSP00000570077.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 587,
"cds_start": 408,
"cds_end": null,
"cds_length": 1764,
"cdna_start": 460,
"cdna_end": null,
"cdna_length": 2178,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900018.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "ENST00000900017.1",
"protein_id": "ENSP00000570076.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 555,
"cds_start": 408,
"cds_end": null,
"cds_length": 1668,
"cdna_start": 460,
"cdna_end": null,
"cdna_length": 3145,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900017.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "ENST00000900016.1",
"protein_id": "ENSP00000570075.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 546,
"cds_start": 408,
"cds_end": null,
"cds_length": 1641,
"cdna_start": 526,
"cdna_end": null,
"cdna_length": 3184,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900016.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "ENST00000924640.1",
"protein_id": "ENSP00000594699.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 542,
"cds_start": 408,
"cds_end": null,
"cds_length": 1629,
"cdna_start": 484,
"cdna_end": null,
"cdna_length": 2077,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924640.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.366A>C",
"hgvs_p": "p.Arg122Ser",
"transcript": "NM_001284222.2",
"protein_id": "NP_001271151.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 533,
"cds_start": 366,
"cds_end": null,
"cds_length": 1602,
"cdna_start": 490,
"cdna_end": null,
"cdna_length": 3154,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284222.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.192A>C",
"hgvs_p": "p.Arg64Ser",
"transcript": "NM_001284220.2",
"protein_id": "NP_001271149.1",
"transcript_support_level": null,
"aa_start": 64,
"aa_end": null,
"aa_length": 475,
"cds_start": 192,
"cds_end": null,
"cds_length": 1428,
"cdna_start": 384,
"cdna_end": null,
"cdna_length": 3048,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284220.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.192A>C",
"hgvs_p": "p.Arg64Ser",
"transcript": "ENST00000524103.5",
"protein_id": "ENSP00000429180.1",
"transcript_support_level": 2,
"aa_start": 64,
"aa_end": null,
"aa_length": 475,
"cds_start": 192,
"cds_end": null,
"cds_length": 1428,
"cdna_start": 411,
"cdna_end": null,
"cdna_length": 1914,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000524103.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.132A>C",
"hgvs_p": "p.Arg44Ser",
"transcript": "NM_001284226.2",
"protein_id": "NP_001271155.1",
"transcript_support_level": null,
"aa_start": 44,
"aa_end": null,
"aa_length": 455,
"cds_start": 132,
"cds_end": null,
"cds_length": 1368,
"cdna_start": 345,
"cdna_end": null,
"cdna_length": 3009,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284226.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.51A>C",
"hgvs_p": "p.Arg17Ser",
"transcript": "NM_001284224.2",
"protein_id": "NP_001271153.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 428,
"cds_start": 51,
"cds_end": null,
"cds_length": 1287,
"cdna_start": 281,
"cdna_end": null,
"cdna_length": 2945,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284224.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.51A>C",
"hgvs_p": "p.Arg17Ser",
"transcript": "NM_001284225.2",
"protein_id": "NP_001271154.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 428,
"cds_start": 51,
"cds_end": null,
"cds_length": 1287,
"cdna_start": 320,
"cdna_end": null,
"cdna_length": 2984,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284225.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.51A>C",
"hgvs_p": "p.Arg17Ser",
"transcript": "ENST00000537665.2",
"protein_id": "ENSP00000445558.1",
"transcript_support_level": 2,
"aa_start": 17,
"aa_end": null,
"aa_length": 428,
"cds_start": 51,
"cds_end": null,
"cds_length": 1287,
"cdna_start": 392,
"cdna_end": null,
"cdna_length": 3053,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000537665.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser",
"transcript": "ENST00000924638.1",
"protein_id": "ENSP00000594697.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 386,
"cds_start": 408,
"cds_end": null,
"cds_length": 1161,
"cdna_start": 480,
"cdna_end": null,
"cdna_length": 2661,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924638.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.366A>C",
"hgvs_p": "p.Arg122Ser",
"transcript": "ENST00000521570.5",
"protein_id": "ENSP00000428532.1",
"transcript_support_level": 5,
"aa_start": 122,
"aa_end": null,
"aa_length": 190,
"cds_start": 366,
"cds_end": null,
"cds_length": 575,
"cdna_start": 447,
"cdna_end": null,
"cdna_length": 656,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000521570.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.366A>C",
"hgvs_p": "p.Arg122Ser",
"transcript": "ENST00000520288.5",
"protein_id": "ENSP00000429248.1",
"transcript_support_level": 4,
"aa_start": 122,
"aa_end": null,
"aa_length": 133,
"cds_start": 366,
"cds_end": null,
"cds_length": 404,
"cdna_start": 528,
"cdna_end": null,
"cdna_length": 566,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000520288.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.366A>C",
"hgvs_p": "p.Arg122Ser",
"transcript": "XM_024447184.2",
"protein_id": "XP_024302952.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 533,
"cds_start": 366,
"cds_end": null,
"cds_length": 1602,
"cdna_start": 561,
"cdna_end": null,
"cdna_length": 3225,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024447184.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "c.393+2408A>C",
"hgvs_p": null,
"transcript": "ENST00000924639.1",
"protein_id": "ENSP00000594698.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 524,
"cds_start": null,
"cds_end": null,
"cds_length": 1575,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3064,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924639.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "n.*131A>C",
"hgvs_p": null,
"transcript": "ENST00000518112.5",
"protein_id": "ENSP00000429465.1",
"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": 2059,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000518112.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "n.*2A>C",
"hgvs_p": null,
"transcript": "ENST00000519261.5",
"protein_id": "ENSP00000428357.1",
"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": 1924,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000519261.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"hgvs_c": "n.475A>C",
"hgvs_p": null,
"transcript": "ENST00000521938.5",
"protein_id": null,
"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": 1004,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000521938.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
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"biotype": "pseudogene",
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},
{
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"feature": "ENST00000523687.5"
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{
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"canonical": false,
"protein_coding": false,
"strand": true,
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],
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"biotype": "pseudogene",
"feature": "ENST00000523760.5"
},
{
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"protein_coding": false,
"strand": true,
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"non_coding_transcript_exon_variant"
],
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"exon_count": 11,
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"biotype": "retained_intron",
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},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
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"gene_symbol": "ELP3",
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"feature": "ENST00000518112.5"
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{
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"strand": true,
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"3_prime_UTR_variant"
],
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"gene_symbol": "ELP3",
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"hgvs_c": "n.*2A>C",
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"transcript": "ENST00000519261.5",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000519261.5"
},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
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"gene_symbol": "ELP3",
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"hgvs_c": "n.*67A>C",
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"transcript": "ENST00000523687.5",
"protein_id": "ENSP00000430253.1",
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"cds_end": null,
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"cdna_start": null,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000523687.5"
}
],
"gene_symbol": "ELP3",
"gene_hgnc_id": 20696,
"dbsnp": null,
"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": 0.7713053226470947,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.436,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.9996,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.14,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 1.963,
"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": 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": "NM_018091.6",
"gene_symbol": "ELP3",
"hgnc_id": 20696,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.408A>C",
"hgvs_p": "p.Arg136Ser"
}
],
"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
}