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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: 16-89686769-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=89686769&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 89686769,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_052988.5",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "NM_052988.5",
"protein_id": "NP_443714.3",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 360,
"cds_start": 59,
"cds_end": null,
"cds_length": 1083,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1767,
"mane_select": "ENST00000353379.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "ENST00000353379.12",
"protein_id": "ENSP00000338673.7",
"transcript_support_level": 1,
"aa_start": 20,
"aa_end": null,
"aa_length": 360,
"cds_start": 59,
"cds_end": null,
"cds_length": 1083,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1767,
"mane_select": "NM_052988.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "ENST00000625631.1",
"protein_id": "ENSP00000486594.1",
"transcript_support_level": 1,
"aa_start": 20,
"aa_end": null,
"aa_length": 42,
"cds_start": 59,
"cds_end": null,
"cds_length": 129,
"cdna_start": 70,
"cdna_end": null,
"cdna_length": 140,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 13,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.-127+10G>C",
"hgvs_p": null,
"transcript": "ENST00000505473.5",
"protein_id": "ENSP00000424415.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 272,
"cds_start": -4,
"cds_end": null,
"cds_length": 819,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1424,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_011523405.4",
"protein_id": "XP_011521707.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 392,
"cds_start": 59,
"cds_end": null,
"cds_length": 1179,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1863,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_011523406.4",
"protein_id": "XP_011521708.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 386,
"cds_start": 59,
"cds_end": null,
"cds_length": 1161,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1845,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_011523407.4",
"protein_id": "XP_011521709.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 375,
"cds_start": 59,
"cds_end": null,
"cds_length": 1128,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1729,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_011523408.4",
"protein_id": "XP_011521710.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 369,
"cds_start": 59,
"cds_end": null,
"cds_length": 1110,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1711,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_006721308.4",
"protein_id": "XP_006721371.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 354,
"cds_start": 59,
"cds_end": null,
"cds_length": 1065,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1749,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_006721310.4",
"protein_id": "XP_006721373.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 343,
"cds_start": 59,
"cds_end": null,
"cds_length": 1032,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1633,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_017023807.3",
"protein_id": "XP_016879296.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 337,
"cds_start": 59,
"cds_end": null,
"cds_length": 1014,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 1615,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "XM_011523417.4",
"protein_id": "XP_011521719.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 261,
"cds_start": 59,
"cds_end": null,
"cds_length": 786,
"cdna_start": 81,
"cdna_end": null,
"cdna_length": 825,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.57G>C",
"hgvs_p": null,
"transcript": "ENST00000378277.8",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 576,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.70G>C",
"hgvs_p": null,
"transcript": "ENST00000472018.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": 2532,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.59G>C",
"hgvs_p": null,
"transcript": "ENST00000502547.5",
"protein_id": "ENSP00000421597.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 551,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.80G>C",
"hgvs_p": null,
"transcript": "ENST00000505733.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 1703,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.59G>C",
"hgvs_p": null,
"transcript": "ENST00000510811.6",
"protein_id": "ENSP00000455976.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1376,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.59G>C",
"hgvs_p": null,
"transcript": "ENST00000512912.5",
"protein_id": "ENSP00000426264.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 658,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LINC02166",
"gene_hgnc_id": 53027,
"hgvs_c": "n.153C>G",
"hgvs_p": null,
"transcript": "ENST00000749100.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 811,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.81G>C",
"hgvs_p": null,
"transcript": "NR_027702.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1694,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "n.81G>C",
"hgvs_p": null,
"transcript": "NR_027703.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
"cdna_end": null,
"cdna_length": 1560,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LINC02166",
"gene_hgnc_id": 53027,
"hgvs_c": "n.144C>G",
"hgvs_p": null,
"transcript": "NR_184149.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 802,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LINC02166",
"gene_hgnc_id": 53027,
"hgvs_c": "n.144C>G",
"hgvs_p": null,
"transcript": "NR_184150.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 755,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
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"gene_symbol": "LINC02166",
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"hgvs_c": "n.-164C>G",
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"transcript": "ENST00000749104.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 473,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LINC02166",
"gene_hgnc_id": 53027,
"hgvs_c": "n.-166C>G",
"hgvs_p": null,
"transcript": "ENST00000749105.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 678,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"hgvs_c": "c.-692G>C",
"hgvs_p": null,
"transcript": "XM_017023810.2",
"protein_id": "XP_016879299.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 272,
"cds_start": -4,
"cds_end": null,
"cds_length": 819,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2044,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CDK10",
"gene_hgnc_id": 1770,
"dbsnp": "rs764194484",
"frequency_reference_population": 0.0000024809556,
"hom_count_reference_population": 0,
"allele_count_reference_population": 4,
"gnomad_exomes_af": 0.00000136971,
"gnomad_genomes_af": 0.0000131477,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.1125028133392334,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.079,
"revel_prediction": "Benign",
"alphamissense_score": 0.1442,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.26,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.656,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_052988.5",
"gene_symbol": "CDK10",
"hgnc_id": 1770,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NR_184149.1",
"gene_symbol": "LINC02166",
"hgnc_id": 53027,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.144C>G",
"hgvs_p": null
}
],
"clinvar_disease": "Inborn genetic diseases",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Inborn genetic diseases",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}