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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: 17-7260947-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=7260947&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 7260947,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001307.6",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "NM_001307.6",
"protein_id": "NP_001298.3",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 697,
"cdna_end": null,
"cdna_length": 1542,
"mane_select": "ENST00000360325.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001307.6"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000360325.11",
"protein_id": "ENSP00000353475.7",
"transcript_support_level": 1,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 697,
"cdna_end": null,
"cdna_length": 1542,
"mane_select": "NM_001307.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000360325.11"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000397317.8",
"protein_id": "ENSP00000396638.3",
"transcript_support_level": 1,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 617,
"cdna_end": null,
"cdna_length": 1228,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000397317.8"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.13C>G",
"hgvs_p": "p.Leu5Val",
"transcript": "ENST00000574070.5",
"protein_id": "ENSP00000460550.1",
"transcript_support_level": 1,
"aa_start": 5,
"aa_end": null,
"aa_length": 98,
"cds_start": 13,
"cds_end": null,
"cds_length": 299,
"cdna_start": 199,
"cdna_end": null,
"cdna_length": 485,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000574070.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"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": "ENSG00000262302",
"gene_hgnc_id": null,
"hgvs_c": "n.223+874C>G",
"hgvs_p": null,
"transcript": "ENST00000577138.1",
"protein_id": "ENSP00000460571.1",
"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": 489,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000577138.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "NM_001185022.2",
"protein_id": "NP_001171951.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 617,
"cdna_end": null,
"cdna_length": 1462,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001185022.2"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888702.1",
"protein_id": "ENSP00000558761.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 702,
"cdna_end": null,
"cdna_length": 2103,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888702.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888703.1",
"protein_id": "ENSP00000558762.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 632,
"cdna_end": null,
"cdna_length": 1242,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888703.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888704.1",
"protein_id": "ENSP00000558763.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 838,
"cdna_end": null,
"cdna_length": 1447,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888704.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888705.1",
"protein_id": "ENSP00000558764.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 1043,
"cdna_end": null,
"cdna_length": 1649,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888705.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888706.1",
"protein_id": "ENSP00000558765.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 1064,
"cdna_end": null,
"cdna_length": 1676,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888706.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888707.1",
"protein_id": "ENSP00000558766.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 625,
"cdna_end": null,
"cdna_length": 1234,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888707.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000888708.1",
"protein_id": "ENSP00000558767.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 681,
"cdna_end": null,
"cdna_length": 1524,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000888708.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000912871.1",
"protein_id": "ENSP00000582930.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 392,
"cdna_end": null,
"cdna_length": 1237,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912871.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000912872.1",
"protein_id": "ENSP00000582931.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 407,
"cdna_end": null,
"cdna_length": 1251,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912872.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000912873.1",
"protein_id": "ENSP00000582932.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 907,
"cdna_end": null,
"cdna_length": 1516,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912873.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000912874.1",
"protein_id": "ENSP00000582933.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 607,
"cdna_end": null,
"cdna_length": 1216,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912874.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000912875.1",
"protein_id": "ENSP00000582934.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 211,
"cds_start": 262,
"cds_end": null,
"cds_length": 636,
"cdna_start": 695,
"cdna_end": null,
"cdna_length": 1301,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912875.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.322C>G",
"hgvs_p": "p.Leu108Val",
"transcript": "ENST00000575313.1",
"protein_id": "ENSP00000460796.1",
"transcript_support_level": 3,
"aa_start": 108,
"aa_end": null,
"aa_length": 192,
"cds_start": 322,
"cds_end": null,
"cds_length": 581,
"cdna_start": 346,
"cdna_end": null,
"cdna_length": 605,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000575313.1"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "NM_001185023.2",
"protein_id": "NP_001171952.1",
"transcript_support_level": null,
"aa_start": 88,
"aa_end": null,
"aa_length": 145,
"cds_start": 262,
"cds_end": null,
"cds_length": 438,
"cdna_start": 697,
"cdna_end": null,
"cdna_length": 1457,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001185023.2"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val",
"transcript": "ENST00000538261.7",
"protein_id": "ENSP00000445131.2",
"transcript_support_level": 5,
"aa_start": 88,
"aa_end": null,
"aa_length": 145,
"cds_start": 262,
"cds_end": null,
"cds_length": 438,
"cdna_start": 1164,
"cdna_end": null,
"cdna_length": 1923,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000538261.7"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLDN7",
"gene_hgnc_id": 2049,
"hgvs_c": "c.236C>G",
"hgvs_p": "p.Pro79Arg",
"transcript": "ENST00000571881.2",
"protein_id": "ENSP00000465963.1",
"transcript_support_level": 3,
"aa_start": 79,
"aa_end": null,
"aa_length": 140,
"cds_start": 236,
"cds_end": null,
"cds_length": 423,
"cdna_start": 536,
"cdna_end": null,
"cdna_length": 735,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000571881.2"
},
{
"aa_ref": "L",
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"protein_coding": true,
"strand": false,
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"missense_variant"
],
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"gene_symbol": "CLDN7",
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"protein_id": "ENSP00000467220.1",
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"aa_start": 88,
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"aa_length": 128,
"cds_start": 262,
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"cds_length": 388,
"cdna_start": 617,
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"cdna_length": 743,
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"biotype": "protein_coding",
"feature": "ENST00000571932.2"
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{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
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"exon_count": 3,
"intron_rank": 1,
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"gene_symbol": "CLDN7",
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"hgvs_c": "c.224-221C>G",
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"transcript": "ENST00000912876.1",
"protein_id": "ENSP00000582935.1",
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"aa_length": 156,
"cds_start": null,
"cds_end": null,
"cds_length": 471,
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"cdna_length": 1377,
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"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912876.1"
}
],
"gene_symbol": "CLDN7",
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"dbsnp": "rs149308129",
"frequency_reference_population": 6.843428e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84343e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.31403136253356934,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.19,
"revel_prediction": "Benign",
"alphamissense_score": 0.0918,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.33,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.838,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.02,
"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": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001307.6",
"gene_symbol": "CLDN7",
"hgnc_id": 2049,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Leu88Val"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000577138.1",
"gene_symbol": "ENSG00000262302",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.223+874C>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
}