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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: 2-105386432-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=105386432&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 105386432,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000530340.6",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_001318895.3",
"protein_id": "NP_001305824.1",
"transcript_support_level": null,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 370,
"cdna_end": null,
"cdna_length": 1582,
"mane_select": "ENST00000530340.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000530340.6",
"protein_id": "ENSP00000433567.2",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 370,
"cdna_end": null,
"cdna_length": 1582,
"mane_select": "NM_001318895.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000322142.13",
"protein_id": "ENSP00000322909.8",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 252,
"cdna_end": null,
"cdna_length": 1478,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000344213.9",
"protein_id": "ENSP00000344266.5",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 664,
"cdna_end": null,
"cdna_length": 1876,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000393352.7",
"protein_id": "ENSP00000377020.3",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 214,
"cdna_end": null,
"cdna_length": 1426,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000393353.7",
"protein_id": "ENSP00000377021.3",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 319,
"cdna_end": null,
"cdna_length": 1531,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000409177.6",
"protein_id": "ENSP00000386892.3",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 555,
"cdna_end": null,
"cdna_length": 4881,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000409807.5",
"protein_id": "ENSP00000386665.1",
"transcript_support_level": 1,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 420,
"cdna_end": null,
"cdna_length": 1601,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.-362G>A",
"hgvs_p": null,
"transcript": "NM_001318899.2",
"protein_id": "NP_001305828.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 171,
"cds_start": -4,
"cds_end": null,
"cds_length": 516,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4690,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.-83G>A",
"hgvs_p": null,
"transcript": "NM_001318897.2",
"protein_id": "NP_001305826.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 165,
"cds_start": -4,
"cds_end": null,
"cds_length": 498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4375,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.-83G>A",
"hgvs_p": null,
"transcript": "NM_001318898.2",
"protein_id": "NP_001305827.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 165,
"cds_start": -4,
"cds_end": null,
"cds_length": 498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4521,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_001039492.3",
"protein_id": "NP_001034581.1",
"transcript_support_level": null,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 242,
"cdna_end": null,
"cdna_length": 4568,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_001318894.1",
"protein_id": "NP_001305823.1",
"transcript_support_level": null,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
"cds_length": 840,
"cdna_start": 555,
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"cdna_length": 1767,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
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"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_001318896.2",
"protein_id": "NP_001305825.1",
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 3,
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"exon_count": 7,
"intron_rank": null,
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"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_001374399.1",
"protein_id": "NP_001361328.1",
"transcript_support_level": null,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
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"cdna_start": 291,
"cdna_end": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "V",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
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"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_001450.4",
"protein_id": "NP_001441.4",
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_201555.3",
"protein_id": "NP_963849.1",
"transcript_support_level": null,
"aa_start": 29,
"aa_end": null,
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"cds_start": 85,
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"cdna_start": 491,
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"cdna_length": 1703,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "NM_201557.5",
"protein_id": "NP_963851.2",
"transcript_support_level": null,
"aa_start": 29,
"aa_end": null,
"aa_length": 279,
"cds_start": 85,
"cds_end": null,
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"cdna_start": 224,
"cdna_end": null,
"cdna_length": 1436,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000408995.5",
"protein_id": "ENSP00000386633.1",
"transcript_support_level": 2,
"aa_start": 29,
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"cds_start": 85,
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},
{
"aa_ref": "V",
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"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000358129.8",
"protein_id": "ENSP00000350846.5",
"transcript_support_level": 5,
"aa_start": 29,
"aa_end": null,
"aa_length": 151,
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"cdna_start": 543,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"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": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met",
"transcript": "ENST00000607522.1",
"protein_id": "ENSP00000476199.1",
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"aa_length": 65,
"cds_start": 85,
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"cdna_start": 224,
"cdna_end": null,
"cdna_length": 759,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "n.85G>A",
"hgvs_p": null,
"transcript": "ENST00000452732.1",
"protein_id": "ENSP00000414872.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 886,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.-362G>A",
"hgvs_p": null,
"transcript": "NM_001318899.2",
"protein_id": "NP_001305828.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 171,
"cds_start": -4,
"cds_end": null,
"cds_length": 516,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4690,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 2,
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"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.-83G>A",
"hgvs_p": null,
"transcript": "NM_001318897.2",
"protein_id": "NP_001305826.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 165,
"cds_start": -4,
"cds_end": null,
"cds_length": 498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4375,
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"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 3,
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"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.-83G>A",
"hgvs_p": null,
"transcript": "NM_001318898.2",
"protein_id": "NP_001305827.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 165,
"cds_start": -4,
"cds_end": null,
"cds_length": 498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4521,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"hgvs_c": "c.*26G>A",
"hgvs_p": null,
"transcript": "ENST00000447958.1",
"protein_id": "ENSP00000397083.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 18,
"cds_start": -4,
"cds_end": null,
"cds_length": 59,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 574,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "FHL2",
"gene_hgnc_id": 3703,
"dbsnp": "rs56284940",
"frequency_reference_population": 0.0014873983,
"hom_count_reference_population": 6,
"allele_count_reference_population": 2401,
"gnomad_exomes_af": 0.0015391,
"gnomad_genomes_af": 0.000991217,
"gnomad_exomes_ac": 2250,
"gnomad_genomes_ac": 151,
"gnomad_exomes_homalt": 5,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.054731518030166626,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.553,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.1724,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.05,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 2.214,
"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": -16,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS2",
"acmg_by_gene": [
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000530340.6",
"gene_symbol": "FHL2",
"hgnc_id": 3703,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.85G>A",
"hgvs_p": "p.Val29Met"
}
],
"clinvar_disease": "Cardiomyopathy,FHL2-related disorder,Primary dilated cardiomyopathy,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2 B:1",
"phenotype_combined": "not specified|Primary dilated cardiomyopathy|Cardiomyopathy|FHL2-related disorder",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}