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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: 22-33283320-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=33283320&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 33283320,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_004737.7",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_133642.5",
"protein_id": "NP_598397.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2323,
"cdna_end": null,
"cdna_length": 4753,
"mane_select": "ENST00000397394.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_133642.5"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000397394.8",
"protein_id": "ENSP00000380549.2",
"transcript_support_level": 5,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2323,
"cdna_end": null,
"cdna_length": 4753,
"mane_select": "NM_133642.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000397394.8"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000354992.7",
"protein_id": "ENSP00000347088.2",
"transcript_support_level": 1,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2331,
"cdna_end": null,
"cdna_length": 4193,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000354992.7"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1603A>G",
"hgvs_p": "p.Asn535Asp",
"transcript": "ENST00000402320.6",
"protein_id": "ENSP00000385223.1",
"transcript_support_level": 1,
"aa_start": 535,
"aa_end": null,
"aa_length": 704,
"cds_start": 1603,
"cds_end": null,
"cds_length": 2115,
"cdna_start": 2105,
"cdna_end": null,
"cdna_length": 3967,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000402320.6"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000911682.1",
"protein_id": "ENSP00000581741.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 779,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2340,
"cdna_start": 2852,
"cdna_end": null,
"cdna_length": 4784,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000911682.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000966032.1",
"protein_id": "ENSP00000636091.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 779,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2340,
"cdna_start": 2926,
"cdna_end": null,
"cdna_length": 4845,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000966032.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_001362949.2",
"protein_id": "NP_001349878.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2108,
"cdna_end": null,
"cdna_length": 4538,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001362949.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_001362951.2",
"protein_id": "NP_001349880.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 1928,
"cdna_end": null,
"cdna_length": 4358,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001362951.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_001362953.2",
"protein_id": "NP_001349882.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2045,
"cdna_end": null,
"cdna_length": 4475,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001362953.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_001378624.1",
"protein_id": "NP_001365553.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 1991,
"cdna_end": null,
"cdna_length": 4421,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001378624.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_001378625.1",
"protein_id": "NP_001365554.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2126,
"cdna_end": null,
"cdna_length": 4556,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001378625.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_001378626.1",
"protein_id": "NP_001365555.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2063,
"cdna_end": null,
"cdna_length": 4493,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001378626.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "NM_004737.7",
"protein_id": "NP_004728.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2386,
"cdna_end": null,
"cdna_length": 4816,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004737.7"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000413114.6",
"protein_id": "ENSP00000415546.2",
"transcript_support_level": 4,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2125,
"cdna_end": null,
"cdna_length": 3987,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000413114.6"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000675416.1",
"protein_id": "ENSP00000502826.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 1962,
"cdna_end": null,
"cdna_length": 3824,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000675416.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000676070.1",
"protein_id": "ENSP00000502152.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2050,
"cdna_end": null,
"cdna_length": 3912,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000676070.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000676132.1",
"protein_id": "ENSP00000501854.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 1960,
"cdna_end": null,
"cdna_length": 3822,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000676132.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000676370.1",
"protein_id": "ENSP00000502238.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 1961,
"cdna_end": null,
"cdna_length": 3823,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000676370.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000899788.1",
"protein_id": "ENSP00000569847.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2313,
"cdna_end": null,
"cdna_length": 4175,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899788.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000899791.1",
"protein_id": "ENSP00000569850.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2238,
"cdna_end": null,
"cdna_length": 4101,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899791.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000899792.1",
"protein_id": "ENSP00000569851.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 756,
"cds_start": 1759,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 2187,
"cdna_end": null,
"cdna_length": 4049,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899792.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LARGE1",
"gene_hgnc_id": 6511,
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp",
"transcript": "ENST00000899793.1",
"protein_id": "ENSP00000569852.1",
"transcript_support_level": null,
"aa_start": 587,
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{
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{
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},
{
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"3_prime_UTR_variant"
],
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"gene_symbol": "LARGE1",
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"hgvs_c": "n.*341A>G",
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"transcript": "ENST00000676031.1",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000676031.1"
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],
"gene_symbol": "LARGE1",
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"dbsnp": "rs749685972",
"frequency_reference_population": 0.000025309737,
"hom_count_reference_population": 0,
"allele_count_reference_population": 37,
"gnomad_exomes_af": 0.0000253097,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 37,
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"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.16258582472801208,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.033,
"revel_prediction": "Benign",
"alphamissense_score": 0.0877,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.57,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.133,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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_004737.7",
"gene_symbol": "LARGE1",
"hgnc_id": 6511,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1759A>G",
"hgvs_p": "p.Asn587Asp"
}
],
"clinvar_disease": "Muscular dystrophy-dystroglycanopathy type B6",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Muscular dystrophy-dystroglycanopathy type B6",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}