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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: 7-861385-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=861385&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 861385,
"ref": "A",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "NM_001367651.1",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.1785A>T",
"hgvs_p": "p.Ala595Ala",
"transcript": "NM_001130965.3",
"protein_id": "NP_001124437.1",
"transcript_support_level": null,
"aa_start": 595,
"aa_end": null,
"aa_length": 785,
"cds_start": 1785,
"cds_end": null,
"cds_length": 2358,
"cdna_start": 1834,
"cdna_end": null,
"cdna_length": 4010,
"mane_select": "ENST00000401592.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130965.3"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.1785A>T",
"hgvs_p": "p.Ala595Ala",
"transcript": "ENST00000401592.6",
"protein_id": "ENSP00000384015.1",
"transcript_support_level": 1,
"aa_start": 595,
"aa_end": null,
"aa_length": 785,
"cds_start": 1785,
"cds_end": null,
"cds_length": 2358,
"cdna_start": 1834,
"cdna_end": null,
"cdna_length": 4010,
"mane_select": "NM_001130965.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000401592.6"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.1560A>T",
"hgvs_p": "p.Ala520Ala",
"transcript": "ENST00000429178.5",
"protein_id": "ENSP00000409909.1",
"transcript_support_level": 1,
"aa_start": 520,
"aa_end": null,
"aa_length": 710,
"cds_start": 1560,
"cds_end": null,
"cds_length": 2133,
"cdna_start": 1560,
"cdna_end": null,
"cdna_length": 3701,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000429178.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "n.1894A>T",
"hgvs_p": null,
"transcript": "ENST00000475971.5",
"protein_id": null,
"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": 4038,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000475971.5"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2442A>T",
"hgvs_p": "p.Ala814Ala",
"transcript": "ENST00000963118.1",
"protein_id": "ENSP00000633177.1",
"transcript_support_level": null,
"aa_start": 814,
"aa_end": null,
"aa_length": 1004,
"cds_start": 2442,
"cds_end": null,
"cds_length": 3015,
"cdna_start": 2495,
"cdna_end": null,
"cdna_length": 4637,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963118.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2409A>T",
"hgvs_p": "p.Ala803Ala",
"transcript": "ENST00000963093.1",
"protein_id": "ENSP00000633151.1",
"transcript_support_level": null,
"aa_start": 803,
"aa_end": null,
"aa_length": 993,
"cds_start": 2409,
"cds_end": null,
"cds_length": 2982,
"cdna_start": 2469,
"cdna_end": null,
"cdna_length": 4613,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963093.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2406A>T",
"hgvs_p": "p.Ala802Ala",
"transcript": "ENST00000963103.1",
"protein_id": "ENSP00000633162.1",
"transcript_support_level": null,
"aa_start": 802,
"aa_end": null,
"aa_length": 992,
"cds_start": 2406,
"cds_end": null,
"cds_length": 2979,
"cdna_start": 2464,
"cdna_end": null,
"cdna_length": 4607,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963103.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2361A>T",
"hgvs_p": "p.Ala787Ala",
"transcript": "ENST00000963140.1",
"protein_id": "ENSP00000633199.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 977,
"cds_start": 2361,
"cds_end": null,
"cds_length": 2934,
"cdna_start": 2411,
"cdna_end": null,
"cdna_length": 4548,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963140.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2358A>T",
"hgvs_p": "p.Ala786Ala",
"transcript": "ENST00000963135.1",
"protein_id": "ENSP00000633194.1",
"transcript_support_level": null,
"aa_start": 786,
"aa_end": null,
"aa_length": 976,
"cds_start": 2358,
"cds_end": null,
"cds_length": 2931,
"cdna_start": 2405,
"cdna_end": null,
"cdna_length": 4549,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963135.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2334A>T",
"hgvs_p": "p.Ala778Ala",
"transcript": "ENST00000963074.1",
"protein_id": "ENSP00000633133.1",
"transcript_support_level": null,
"aa_start": 778,
"aa_end": null,
"aa_length": 968,
"cds_start": 2334,
"cds_end": null,
"cds_length": 2907,
"cdna_start": 2408,
"cdna_end": null,
"cdna_length": 4562,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963074.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2331A>T",
"hgvs_p": "p.Ala777Ala",
"transcript": "ENST00000963082.1",
"protein_id": "ENSP00000633141.1",
"transcript_support_level": null,
"aa_start": 777,
"aa_end": null,
"aa_length": 967,
"cds_start": 2331,
"cds_end": null,
"cds_length": 2904,
"cdna_start": 2398,
"cdna_end": null,
"cdna_length": 4542,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963082.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2325A>T",
"hgvs_p": "p.Ala775Ala",
"transcript": "ENST00000963107.1",
"protein_id": "ENSP00000633166.1",
"transcript_support_level": null,
"aa_start": 775,
"aa_end": null,
"aa_length": 965,
"cds_start": 2325,
"cds_end": null,
"cds_length": 2898,
"cdna_start": 2374,
"cdna_end": null,
"cdna_length": 4524,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963107.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2298A>T",
"hgvs_p": "p.Ala766Ala",
"transcript": "ENST00000963079.1",
"protein_id": "ENSP00000633138.1",
"transcript_support_level": null,
"aa_start": 766,
"aa_end": null,
"aa_length": 956,
"cds_start": 2298,
"cds_end": null,
"cds_length": 2871,
"cdna_start": 2364,
"cdna_end": null,
"cdna_length": 4516,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963079.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2295A>T",
"hgvs_p": "p.Ala765Ala",
"transcript": "ENST00000881164.1",
"protein_id": "ENSP00000551223.1",
"transcript_support_level": null,
"aa_start": 765,
"aa_end": null,
"aa_length": 955,
"cds_start": 2295,
"cds_end": null,
"cds_length": 2868,
"cdna_start": 2346,
"cdna_end": null,
"cdna_length": 4490,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881164.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2265A>T",
"hgvs_p": "p.Ala755Ala",
"transcript": "ENST00000881168.1",
"protein_id": "ENSP00000551227.1",
"transcript_support_level": null,
"aa_start": 755,
"aa_end": null,
"aa_length": 945,
"cds_start": 2265,
"cds_end": null,
"cds_length": 2838,
"cdna_start": 2316,
"cdna_end": null,
"cdna_length": 4459,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881168.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2331A>T",
"hgvs_p": "p.Ala777Ala",
"transcript": "ENST00000963137.1",
"protein_id": "ENSP00000633196.1",
"transcript_support_level": null,
"aa_start": 777,
"aa_end": null,
"aa_length": 936,
"cds_start": 2331,
"cds_end": null,
"cds_length": 2811,
"cdna_start": 2381,
"cdna_end": null,
"cdna_length": 4428,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963137.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2232A>T",
"hgvs_p": "p.Ala744Ala",
"transcript": "ENST00000963102.1",
"protein_id": "ENSP00000633161.1",
"transcript_support_level": null,
"aa_start": 744,
"aa_end": null,
"aa_length": 934,
"cds_start": 2232,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 2290,
"cdna_end": null,
"cdna_length": 4434,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963102.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2199A>T",
"hgvs_p": "p.Ala733Ala",
"transcript": "NM_001367651.1",
"protein_id": "NP_001354580.1",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 923,
"cds_start": 2199,
"cds_end": null,
"cds_length": 2772,
"cdna_start": 2274,
"cdna_end": null,
"cdna_length": 4450,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001367651.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2199A>T",
"hgvs_p": "p.Ala733Ala",
"transcript": "ENST00000963124.1",
"protein_id": "ENSP00000633183.1",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 923,
"cds_start": 2199,
"cds_end": null,
"cds_length": 2772,
"cdna_start": 2249,
"cdna_end": null,
"cdna_length": 4393,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963124.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2196A>T",
"hgvs_p": "p.Ala732Ala",
"transcript": "ENST00000963113.1",
"protein_id": "ENSP00000633172.1",
"transcript_support_level": null,
"aa_start": 732,
"aa_end": null,
"aa_length": 922,
"cds_start": 2196,
"cds_end": null,
"cds_length": 2769,
"cdna_start": 2247,
"cdna_end": null,
"cdna_length": 4391,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963113.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2178A>T",
"hgvs_p": "p.Ala726Ala",
"transcript": "NM_001367705.1",
"protein_id": "NP_001354634.1",
"transcript_support_level": null,
"aa_start": 726,
"aa_end": null,
"aa_length": 916,
"cds_start": 2178,
"cds_end": null,
"cds_length": 2751,
"cdna_start": 2229,
"cdna_end": null,
"cdna_length": 4405,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001367705.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SUN1",
"gene_hgnc_id": 18587,
"hgvs_c": "c.2175A>T",
"hgvs_p": "p.Ala725Ala",
"transcript": "NM_001367678.1",
"protein_id": "NP_001354607.1",
"transcript_support_level": null,
"aa_start": 725,
"aa_end": null,
"aa_length": 915,
"cds_start": 2175,
"cds_end": null,
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}
],
"message": null
}