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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: 11-65540929-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=65540929&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 65540929,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001130144.3",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2919C>G",
"hgvs_p": "p.Asp973Glu",
"transcript": "NM_001130144.3",
"protein_id": "NP_001123616.1",
"transcript_support_level": null,
"aa_start": 973,
"aa_end": null,
"aa_length": 1303,
"cds_start": 2919,
"cds_end": null,
"cds_length": 3912,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000301873.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130144.3"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2919C>G",
"hgvs_p": "p.Asp973Glu",
"transcript": "ENST00000301873.11",
"protein_id": "ENSP00000301873.5",
"transcript_support_level": 2,
"aa_start": 973,
"aa_end": null,
"aa_length": 1303,
"cds_start": 2919,
"cds_end": null,
"cds_length": 3912,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001130144.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000301873.11"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2919C>G",
"hgvs_p": "p.Asp973Glu",
"transcript": "ENST00000322147.8",
"protein_id": "ENSP00000326647.4",
"transcript_support_level": 1,
"aa_start": 973,
"aa_end": null,
"aa_length": 1256,
"cds_start": 2919,
"cds_end": null,
"cds_length": 3771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000322147.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2564C>G",
"hgvs_p": null,
"transcript": "ENST00000528516.5",
"protein_id": "ENSP00000432350.1",
"transcript_support_level": 1,
"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": "ENST00000528516.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2564C>G",
"hgvs_p": null,
"transcript": "ENST00000528516.5",
"protein_id": "ENSP00000432350.1",
"transcript_support_level": 1,
"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": "ENST00000528516.5"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2946C>G",
"hgvs_p": "p.Asp982Glu",
"transcript": "ENST00000971648.1",
"protein_id": "ENSP00000641707.1",
"transcript_support_level": null,
"aa_start": 982,
"aa_end": null,
"aa_length": 1312,
"cds_start": 2946,
"cds_end": null,
"cds_length": 3939,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971648.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2916C>G",
"hgvs_p": "p.Asp972Glu",
"transcript": "ENST00000971647.1",
"protein_id": "ENSP00000641706.1",
"transcript_support_level": null,
"aa_start": 972,
"aa_end": null,
"aa_length": 1302,
"cds_start": 2916,
"cds_end": null,
"cds_length": 3909,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971647.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2829C>G",
"hgvs_p": "p.Asp943Glu",
"transcript": "ENST00000971650.1",
"protein_id": "ENSP00000641709.1",
"transcript_support_level": null,
"aa_start": 943,
"aa_end": null,
"aa_length": 1273,
"cds_start": 2829,
"cds_end": null,
"cds_length": 3822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971650.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2796C>G",
"hgvs_p": "p.Asp932Glu",
"transcript": "ENST00000689505.1",
"protein_id": "ENSP00000510401.1",
"transcript_support_level": null,
"aa_start": 932,
"aa_end": null,
"aa_length": 1262,
"cds_start": 2796,
"cds_end": null,
"cds_length": 3789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000689505.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2796C>G",
"hgvs_p": "p.Asp932Glu",
"transcript": "ENST00000971646.1",
"protein_id": "ENSP00000641705.1",
"transcript_support_level": null,
"aa_start": 932,
"aa_end": null,
"aa_length": 1262,
"cds_start": 2796,
"cds_end": null,
"cds_length": 3789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971646.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2796C>G",
"hgvs_p": "p.Asp932Glu",
"transcript": "ENST00000971649.1",
"protein_id": "ENSP00000641708.1",
"transcript_support_level": null,
"aa_start": 932,
"aa_end": null,
"aa_length": 1262,
"cds_start": 2796,
"cds_end": null,
"cds_length": 3789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971649.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2919C>G",
"hgvs_p": "p.Asp973Glu",
"transcript": "NM_021070.4",
"protein_id": "NP_066548.2",
"transcript_support_level": null,
"aa_start": 973,
"aa_end": null,
"aa_length": 1256,
"cds_start": 2919,
"cds_end": null,
"cds_length": 3771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_021070.4"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2652C>G",
"hgvs_p": "p.Asp884Glu",
"transcript": "ENST00000530866.6",
"protein_id": "ENSP00000435276.2",
"transcript_support_level": 2,
"aa_start": 884,
"aa_end": null,
"aa_length": 1214,
"cds_start": 2652,
"cds_end": null,
"cds_length": 3645,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000530866.6"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2568C>G",
"hgvs_p": "p.Asp856Glu",
"transcript": "NM_001164266.1",
"protein_id": "NP_001157738.1",
"transcript_support_level": null,
"aa_start": 856,
"aa_end": null,
"aa_length": 1139,
"cds_start": 2568,
"cds_end": null,
"cds_length": 3420,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001164266.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2064C>G",
"hgvs_p": "p.Asp688Glu",
"transcript": "ENST00000526927.6",
"protein_id": "ENSP00000431219.2",
"transcript_support_level": 2,
"aa_start": 688,
"aa_end": null,
"aa_length": 971,
"cds_start": 2064,
"cds_end": null,
"cds_length": 2916,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000526927.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.215C>G",
"hgvs_p": null,
"transcript": "ENST00000526124.1",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000526124.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2182C>G",
"hgvs_p": null,
"transcript": "ENST00000526825.6",
"protein_id": "ENSP00000435146.2",
"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": "ENST00000526825.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.884C>G",
"hgvs_p": null,
"transcript": "ENST00000529189.5",
"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": "retained_intron",
"feature": "ENST00000529189.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.961C>G",
"hgvs_p": null,
"transcript": "ENST00000529582.6",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000529582.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.1207C>G",
"hgvs_p": null,
"transcript": "ENST00000530785.5",
"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": "ENST00000530785.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.2073C>G",
"hgvs_p": null,
"transcript": "ENST00000532932.5",
"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": "retained_intron",
"feature": "ENST00000532932.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.2591C>G",
"hgvs_p": null,
"transcript": "ENST00000685178.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000685178.1"
},
{
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"canonical": false,
"protein_coding": false,
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],
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"exon_count": 16,
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"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000688764.1"
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{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 20,
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"exon_count": 27,
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"gene_symbol": "LTBP3",
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"hgvs_c": "n.*2182C>G",
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"transcript": "ENST00000526825.6",
"protein_id": "ENSP00000435146.2",
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"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000526825.6"
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{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
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"exon_count": 6,
"intron_rank": null,
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"gene_symbol": "LTBP3",
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"hgvs_c": "c.-329C>G",
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"transcript": "ENST00000532661.6",
"protein_id": "ENSP00000436341.2",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 259,
"cds_start": null,
"cds_end": null,
"cds_length": 780,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000532661.6"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
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"exon_count": 2,
"intron_rank": null,
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"gene_symbol": "LTBP3",
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"hgvs_c": "n.*66C>G",
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"transcript": "ENST00000530990.1",
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"transcript_support_level": 2,
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"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": "retained_intron",
"feature": "ENST00000530990.1"
}
],
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"dbsnp": "rs145041278",
"frequency_reference_population": 0.00009296053,
"hom_count_reference_population": 0,
"allele_count_reference_population": 150,
"gnomad_exomes_af": 0.0000917006,
"gnomad_genomes_af": 0.000105049,
"gnomad_exomes_ac": 134,
"gnomad_genomes_ac": 16,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.18099018931388855,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.424,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.3256,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.16,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.145,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_001130144.3",
"gene_symbol": "LTBP3",
"hgnc_id": 6716,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.2919C>G",
"hgvs_p": "p.Asp973Glu"
}
],
"clinvar_disease": "Brachyolmia-amelogenesis imperfecta syndrome,Inborn genetic diseases",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"phenotype_combined": "Brachyolmia-amelogenesis imperfecta syndrome|Inborn genetic diseases",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}