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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: 7-150856540-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=150856540&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 150856540,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001272072.2",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "NM_001091.4",
"protein_id": "NP_001082.2",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 128,
"cdna_end": null,
"cdna_length": 2609,
"mane_select": "ENST00000360937.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001091.4"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000360937.9",
"protein_id": "ENSP00000354193.4",
"transcript_support_level": 1,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 128,
"cdna_end": null,
"cdna_length": 2609,
"mane_select": "NM_001091.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000360937.9"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000416793.6",
"protein_id": "ENSP00000411613.2",
"transcript_support_level": 1,
"aa_start": 24,
"aa_end": null,
"aa_length": 770,
"cds_start": 70,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 130,
"cdna_end": null,
"cdna_length": 2453,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000416793.6"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "NM_001272072.2",
"protein_id": "NP_001259001.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 770,
"cds_start": 70,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 128,
"cdna_end": null,
"cdna_length": 2666,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001272072.2"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000941409.1",
"protein_id": "ENSP00000611468.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 770,
"cds_start": 70,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 203,
"cdna_end": null,
"cdna_length": 2527,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941409.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000467291.5",
"protein_id": "ENSP00000418328.1",
"transcript_support_level": 5,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 376,
"cdna_end": null,
"cdna_length": 2857,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000467291.5"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000493429.5",
"protein_id": "ENSP00000418614.1",
"transcript_support_level": 5,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 654,
"cdna_end": null,
"cdna_length": 3135,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000493429.5"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000863992.1",
"protein_id": "ENSP00000534051.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 157,
"cdna_end": null,
"cdna_length": 2423,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863992.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000863993.1",
"protein_id": "ENSP00000534052.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 211,
"cdna_end": null,
"cdna_length": 2477,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863993.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000863994.1",
"protein_id": "ENSP00000534053.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 121,
"cdna_end": null,
"cdna_length": 2387,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863994.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000941408.1",
"protein_id": "ENSP00000611467.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 395,
"cdna_end": null,
"cdna_length": 2660,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941408.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000483043.1",
"protein_id": "ENSP00000417392.1",
"transcript_support_level": 4,
"aa_start": 24,
"aa_end": null,
"aa_length": 336,
"cds_start": 70,
"cds_end": null,
"cds_length": 1012,
"cdna_start": 372,
"cdna_end": null,
"cdna_length": 1314,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000483043.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "ENST00000460213.1",
"protein_id": "ENSP00000418557.1",
"transcript_support_level": 5,
"aa_start": 24,
"aa_end": null,
"aa_length": 248,
"cds_start": 70,
"cds_end": null,
"cds_length": 747,
"cdna_start": 268,
"cdna_end": null,
"cdna_length": 945,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000460213.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "XM_017011945.2",
"protein_id": "XP_016867434.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 770,
"cds_start": 70,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 157,
"cdna_end": null,
"cdna_length": 2695,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017011945.2"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "XM_017011946.3",
"protein_id": "XP_016867435.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 770,
"cds_start": 70,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 146,
"cdna_end": null,
"cdna_length": 2684,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017011946.3"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "XM_017011947.2",
"protein_id": "XP_016867436.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 146,
"cdna_end": null,
"cdna_length": 2627,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017011947.2"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg",
"transcript": "XM_047420128.1",
"protein_id": "XP_047276084.1",
"transcript_support_level": null,
"aa_start": 24,
"aa_end": null,
"aa_length": 751,
"cds_start": 70,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 157,
"cdna_end": null,
"cdna_length": 2638,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420128.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000289052",
"gene_hgnc_id": null,
"hgvs_c": "n.270+20469C>T",
"hgvs_p": null,
"transcript": "ENST00000726369.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": 788,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000726369.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000289052",
"gene_hgnc_id": null,
"hgvs_c": "n.262-15095C>T",
"hgvs_p": null,
"transcript": "ENST00000726370.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000726370.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000289052",
"gene_hgnc_id": null,
"hgvs_c": "n.262-15095C>T",
"hgvs_p": null,
"transcript": "ENST00000726371.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
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"cds_length": null,
"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000726371.1"
},
{
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"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000289052",
"gene_hgnc_id": null,
"hgvs_c": "n.252+20469C>T",
"hgvs_p": null,
"transcript": "ENST00000726372.1",
"protein_id": null,
"transcript_support_level": null,
"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": 1111,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000726372.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "LOC105375567",
"gene_hgnc_id": null,
"hgvs_c": "n.123-15095C>T",
"hgvs_p": null,
"transcript": "XR_928169.3",
"protein_id": null,
"transcript_support_level": null,
"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": 1855,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_928169.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "LOC105375567",
"gene_hgnc_id": null,
"hgvs_c": "n.123-15095C>T",
"hgvs_p": null,
"transcript": "XR_928171.3",
"protein_id": null,
"transcript_support_level": null,
"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": 5477,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_928171.3"
}
],
"gene_symbol": "AOC1",
"gene_hgnc_id": 80,
"dbsnp": "rs373918366",
"frequency_reference_population": 0.000008054533,
"hom_count_reference_population": 1,
"allele_count_reference_population": 13,
"gnomad_exomes_af": 0.0000082089,
"gnomad_genomes_af": 0.0000065716,
"gnomad_exomes_ac": 12,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.052097827196121216,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.017,
"revel_prediction": "Benign",
"alphamissense_score": 0.0684,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.68,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -4.429,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong,BP6_Moderate",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 6,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_001272072.2",
"gene_symbol": "AOC1",
"hgnc_id": 80,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.70G>A",
"hgvs_p": "p.Gly24Arg"
},
{
"score": -4,
"benign_score": 6,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000726369.1",
"gene_symbol": "ENSG00000289052",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.270+20469C>T",
"hgvs_p": null
},
{
"score": -4,
"benign_score": 6,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "XR_928169.3",
"gene_symbol": "LOC105375567",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.123-15095C>T",
"hgvs_p": null
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}