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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: 17-8369571-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=8369571&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 8369571,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_213597.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRABD2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "NM_001304947.3",
"protein_id": "NP_001291876.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000396267.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001304947.3"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000396267.3",
"protein_id": "ENSP00000379565.3",
"transcript_support_level": 2,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001304947.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000396267.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"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": "ENSG00000263809",
"gene_hgnc_id": null,
"hgvs_c": "n.*1779G>C",
"hgvs_p": null,
"transcript": "ENST00000582471.1",
"protein_id": "ENSP00000463847.1",
"transcript_support_level": 5,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000582471.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000263809",
"gene_hgnc_id": null,
"hgvs_c": "n.*1779G>C",
"hgvs_p": null,
"transcript": "ENST00000582471.1",
"protein_id": "ENSP00000463847.1",
"transcript_support_level": 5,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000582471.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRABD2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.1042G>C",
"hgvs_p": "p.Val348Leu",
"transcript": "NM_213597.3",
"protein_id": "NP_998762.1",
"transcript_support_level": null,
"aa_start": 348,
"aa_end": null,
"aa_length": 492,
"cds_start": 1042,
"cds_end": null,
"cds_length": 1479,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_213597.3"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.1042G>C",
"hgvs_p": "p.Val348Leu",
"transcript": "ENST00000643221.1",
"protein_id": "ENSP00000494883.1",
"transcript_support_level": null,
"aa_start": 348,
"aa_end": null,
"aa_length": 492,
"cds_start": 1042,
"cds_end": null,
"cds_length": 1479,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000643221.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.940G>C",
"hgvs_p": "p.Val314Leu",
"transcript": "ENST00000647210.1",
"protein_id": "ENSP00000496270.1",
"transcript_support_level": null,
"aa_start": 314,
"aa_end": null,
"aa_length": 458,
"cds_start": 940,
"cds_end": null,
"cds_length": 1377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000647210.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.940G>C",
"hgvs_p": "p.Val314Leu",
"transcript": "ENST00000649935.1",
"protein_id": "ENSP00000496946.1",
"transcript_support_level": null,
"aa_start": 314,
"aa_end": null,
"aa_length": 458,
"cds_start": 940,
"cds_end": null,
"cds_length": 1377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649935.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000851333.1",
"protein_id": "ENSP00000521392.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851333.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000851334.1",
"protein_id": "ENSP00000521393.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851334.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952554.1",
"protein_id": "ENSP00000622613.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952554.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952555.1",
"protein_id": "ENSP00000622614.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952555.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952556.1",
"protein_id": "ENSP00000622615.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952556.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952557.1",
"protein_id": "ENSP00000622616.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952557.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952558.1",
"protein_id": "ENSP00000622617.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952558.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952559.1",
"protein_id": "ENSP00000622618.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952559.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952560.1",
"protein_id": "ENSP00000622619.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952560.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KRBA2",
"gene_hgnc_id": 26989,
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu",
"transcript": "ENST00000952561.1",
"protein_id": "ENSP00000622620.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 410,
"cds_start": 796,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952561.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000265749",
"gene_hgnc_id": null,
"hgvs_c": "n.153+3850C>G",
"hgvs_p": null,
"transcript": "ENST00000579904.6",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000579904.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000265749",
"gene_hgnc_id": null,
"hgvs_c": "n.153+3850C>G",
"hgvs_p": null,
"transcript": "ENST00000580537.1",
"protein_id": null,
"transcript_support_level": 3,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000580537.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ENSG00000265749",
"gene_hgnc_id": null,
"hgvs_c": "n.205+2363C>G",
"hgvs_p": null,
"transcript": "ENST00000583963.1",
"protein_id": null,
"transcript_support_level": 4,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000583963.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000265749",
"gene_hgnc_id": null,
"hgvs_c": "n.158+3850C>G",
"hgvs_p": null,
"transcript": "ENST00000666354.2",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000666354.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
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"gene_symbol": "ENSG00000265749",
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"hgvs_c": "n.199+2363C>G",
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"transcript": "ENST00000774784.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000774784.1"
}
],
"gene_symbol": "KRABD2",
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"dbsnp": "rs976706665",
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"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
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"gnomad_genomes_af": 0.00000656987,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.37623050808906555,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.1,
"revel_prediction": "Benign",
"alphamissense_score": 0.1889,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.45,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.141,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
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"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_213597.3",
"gene_symbol": "KRABD2",
"hgnc_id": 26989,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1042G>C",
"hgvs_p": "p.Val348Leu"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000396267.3",
"gene_symbol": "KRBA2",
"hgnc_id": 26989,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.796G>C",
"hgvs_p": "p.Val266Leu"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000582471.1",
"gene_symbol": "ENSG00000263809",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.*1779G>C",
"hgvs_p": null
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000579904.6",
"gene_symbol": "ENSG00000265749",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.153+3850C>G",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}