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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: 17-63710537-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=63710537&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 63710537,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000336174.12",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.535G>A",
"hgvs_p": "p.Val179Met",
"transcript": "NM_001003787.4",
"protein_id": "NP_001003787.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 431,
"cds_start": 535,
"cds_end": null,
"cds_length": 1296,
"cdna_start": 638,
"cdna_end": null,
"cdna_length": 2166,
"mane_select": "ENST00000336174.12",
"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": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.535G>A",
"hgvs_p": "p.Val179Met",
"transcript": "ENST00000336174.12",
"protein_id": "ENSP00000336655.6",
"transcript_support_level": 1,
"aa_start": 179,
"aa_end": null,
"aa_length": 431,
"cds_start": 535,
"cds_end": null,
"cds_length": 1296,
"cdna_start": 638,
"cdna_end": null,
"cdna_length": 2166,
"mane_select": "NM_001003787.4",
"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": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.361G>A",
"hgvs_p": "p.Val121Met",
"transcript": "ENST00000375840.9",
"protein_id": "ENSP00000365000.4",
"transcript_support_level": 1,
"aa_start": 121,
"aa_end": null,
"aa_length": 373,
"cds_start": 361,
"cds_end": null,
"cds_length": 1122,
"cdna_start": 684,
"cdna_end": null,
"cdna_length": 2209,
"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": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Met",
"transcript": "ENST00000392950.9",
"protein_id": "ENSP00000376677.4",
"transcript_support_level": 1,
"aa_start": 142,
"aa_end": null,
"aa_length": 348,
"cds_start": 424,
"cds_end": null,
"cds_length": 1047,
"cdna_start": 714,
"cdna_end": null,
"cdna_length": 2778,
"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": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.361G>A",
"hgvs_p": "p.Val121Met",
"transcript": "ENST00000245865.10",
"protein_id": "ENSP00000245865.5",
"transcript_support_level": 1,
"aa_start": 121,
"aa_end": null,
"aa_length": 234,
"cds_start": 361,
"cds_end": null,
"cds_length": 705,
"cdna_start": 571,
"cdna_end": null,
"cdna_length": 2959,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 12,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "ENSG00000125695",
"gene_hgnc_id": null,
"hgvs_c": "n.*495+191G>A",
"hgvs_p": null,
"transcript": "ENST00000580553.1",
"protein_id": "ENSP00000464100.1",
"transcript_support_level": 5,
"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": 2128,
"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": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.511G>A",
"hgvs_p": "p.Val171Met",
"transcript": "NM_001363786.1",
"protein_id": "NP_001350715.1",
"transcript_support_level": null,
"aa_start": 171,
"aa_end": null,
"aa_length": 423,
"cds_start": 511,
"cds_end": null,
"cds_length": 1272,
"cdna_start": 801,
"cdna_end": null,
"cdna_length": 2329,
"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": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.535G>A",
"hgvs_p": "p.Val179Met",
"transcript": "ENST00000638193.1",
"protein_id": "ENSP00000491928.1",
"transcript_support_level": 5,
"aa_start": 179,
"aa_end": null,
"aa_length": 403,
"cds_start": 535,
"cds_end": null,
"cds_length": 1212,
"cdna_start": 638,
"cdna_end": null,
"cdna_length": 1342,
"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": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Met",
"transcript": "NM_001363787.1",
"protein_id": "NP_001350716.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 402,
"cds_start": 448,
"cds_end": null,
"cds_length": 1209,
"cdna_start": 738,
"cdna_end": null,
"cdna_length": 2266,
"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": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Met",
"transcript": "ENST00000638708.1",
"protein_id": "ENSP00000491580.1",
"transcript_support_level": 2,
"aa_start": 150,
"aa_end": null,
"aa_length": 402,
"cds_start": 448,
"cds_end": null,
"cds_length": 1209,
"cdna_start": 612,
"cdna_end": null,
"cdna_length": 2153,
"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": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Met",
"transcript": "NM_001003786.3",
"protein_id": "NP_001003786.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 394,
"cds_start": 424,
"cds_end": null,
"cds_length": 1185,
"cdna_start": 714,
"cdna_end": null,
"cdna_length": 2242,
"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": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
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"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Met",
"transcript": "ENST00000639835.1",
"protein_id": "ENSP00000492578.1",
"transcript_support_level": 2,
"aa_start": 142,
"aa_end": null,
"aa_length": 394,
"cds_start": 424,
"cds_end": null,
"cds_length": 1185,
"cdna_start": 589,
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"cdna_length": 2130,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
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"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Met",
"transcript": "ENST00000640999.1",
"protein_id": "ENSP00000491643.1",
"transcript_support_level": 5,
"aa_start": 142,
"aa_end": null,
"aa_length": 394,
"cds_start": 424,
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"cds_length": 1185,
"cdna_start": 811,
"cdna_end": null,
"cdna_length": 2336,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
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"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.361G>A",
"hgvs_p": "p.Val121Met",
"transcript": "NM_001003788.3",
"protein_id": "NP_001003788.1",
"transcript_support_level": null,
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},
{
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"consequences": [
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],
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"intron_rank": null,
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"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.361G>A",
"hgvs_p": "p.Val121Met",
"transcript": "ENST00000638702.1",
"protein_id": "ENSP00000491017.1",
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"aa_start": 121,
"aa_end": null,
"aa_length": 373,
"cds_start": 361,
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"cdna_start": 618,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 6,
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"exon_count": 9,
"intron_rank": null,
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"gene_symbol": "STRADA",
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"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Met",
"transcript": "NM_153335.6",
"protein_id": "NP_699166.2",
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},
{
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],
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"intron_rank": null,
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"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.361G>A",
"hgvs_p": "p.Val121Met",
"transcript": "ENST00000640979.1",
"protein_id": "ENSP00000491485.1",
"transcript_support_level": 5,
"aa_start": 121,
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"aa_length": 345,
"cds_start": 361,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
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"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.535G>A",
"hgvs_p": "p.Val179Met",
"transcript": "NM_001363788.1",
"protein_id": "NP_001350717.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 343,
"cds_start": 535,
"cds_end": null,
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"cdna_start": 825,
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"mane_select": null,
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"biotype": null,
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": 8,
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"exon_count": 13,
"intron_rank": null,
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"gene_symbol": "STRADA",
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"hgvs_c": "c.535G>A",
"hgvs_p": "p.Val179Met",
"transcript": "ENST00000638888.1",
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},
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],
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"intron_rank": null,
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"gene_symbol": "STRADA",
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"hgvs_c": "c.535G>A",
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"transcript": "ENST00000638698.1",
"protein_id": "ENSP00000491082.1",
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"aa_end": null,
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"feature": null
},
{
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"strand": false,
"consequences": [
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],
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"intron_rank": null,
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"gene_symbol": "STRADA",
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"transcript": "ENST00000640679.1",
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.511G>A",
"hgvs_p": "p.Val171Met",
"transcript": "ENST00000640174.1",
"protein_id": "ENSP00000491380.1",
"transcript_support_level": 5,
"aa_start": 171,
"aa_end": null,
"aa_length": 324,
"cds_start": 511,
"cds_end": null,
"cds_length": 976,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 1125,
"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": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRADA",
"gene_hgnc_id": 30172,
"hgvs_c": "c.448G>A",
"hgvs_p": "p.Val150Met",
"transcript": "NM_001165969.2",
"protein_id": "NP_001159441.1",
"transcript_support_level": null,
"aa_start": 150,
"aa_end": null,
"aa_length": 314,
"cds_start": 448,
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}