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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: 12-55697492-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=55697492&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 55697492,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000257879.11",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1464C>T",
          "hgvs_p": "p.Ile488Ile",
          "transcript": "NM_002206.3",
          "protein_id": "NP_002197.2",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 1137,
          "cds_start": 1464,
          "cds_end": null,
          "cds_length": 3414,
          "cdna_start": 1686,
          "cdna_end": null,
          "cdna_length": 4126,
          "mane_select": "ENST00000257879.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1464C>T",
          "hgvs_p": "p.Ile488Ile",
          "transcript": "ENST00000257879.11",
          "protein_id": "ENSP00000257879.7",
          "transcript_support_level": 1,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 1137,
          "cds_start": 1464,
          "cds_end": null,
          "cds_length": 3414,
          "cdna_start": 1686,
          "cdna_end": null,
          "cdna_length": 4126,
          "mane_select": "NM_002206.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1476C>T",
          "hgvs_p": "p.Ile492Ile",
          "transcript": "ENST00000553804.6",
          "protein_id": "ENSP00000452120.1",
          "transcript_support_level": 1,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 1141,
          "cds_start": 1476,
          "cds_end": null,
          "cds_length": 3426,
          "cdna_start": 1698,
          "cdna_end": null,
          "cdna_length": 4138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1596C>T",
          "hgvs_p": "p.Ile532Ile",
          "transcript": "NM_001410977.1",
          "protein_id": "NP_001397906.1",
          "transcript_support_level": null,
          "aa_start": 532,
          "aa_end": null,
          "aa_length": 1181,
          "cds_start": 1596,
          "cds_end": null,
          "cds_length": 3546,
          "cdna_start": 1818,
          "cdna_end": null,
          "cdna_length": 4258,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1596C>T",
          "hgvs_p": "p.Ile532Ile",
          "transcript": "ENST00000555728.5",
          "protein_id": "ENSP00000452387.1",
          "transcript_support_level": 5,
          "aa_start": 532,
          "aa_end": null,
          "aa_length": 1181,
          "cds_start": 1596,
          "cds_end": null,
          "cds_length": 3546,
          "cdna_start": 1625,
          "cdna_end": null,
          "cdna_length": 3930,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1476C>T",
          "hgvs_p": "p.Ile492Ile",
          "transcript": "NM_001144996.2",
          "protein_id": "NP_001138468.1",
          "transcript_support_level": null,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 1141,
          "cds_start": 1476,
          "cds_end": null,
          "cds_length": 3426,
          "cdna_start": 1698,
          "cdna_end": null,
          "cdna_length": 4138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1476C>T",
          "hgvs_p": "p.Ile492Ile",
          "transcript": "NM_001414029.1",
          "protein_id": "NP_001400958.1",
          "transcript_support_level": null,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 1135,
          "cds_start": 1476,
          "cds_end": null,
          "cds_length": 3408,
          "cdna_start": 1698,
          "cdna_end": null,
          "cdna_length": 4120,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1464C>T",
          "hgvs_p": "p.Ile488Ile",
          "transcript": "NM_001374465.1",
          "protein_id": "NP_001361394.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 1131,
          "cds_start": 1464,
          "cds_end": null,
          "cds_length": 3396,
          "cdna_start": 1686,
          "cdna_end": null,
          "cdna_length": 4108,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1464C>T",
          "hgvs_p": "p.Ile488Ile",
          "transcript": "ENST00000347027.10",
          "protein_id": "ENSP00000343009.6",
          "transcript_support_level": 5,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 1131,
          "cds_start": 1464,
          "cds_end": null,
          "cds_length": 3396,
          "cdna_start": 1666,
          "cdna_end": null,
          "cdna_length": 4084,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1476C>T",
          "hgvs_p": "p.Ile492Ile",
          "transcript": "ENST00000557555.3",
          "protein_id": "ENSP00000451039.3",
          "transcript_support_level": 5,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": 1476,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": 1476,
          "cdna_end": null,
          "cdna_length": 3739,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1476C>T",
          "hgvs_p": "p.Ile492Ile",
          "transcript": "ENST00000691973.1",
          "protein_id": "ENSP00000509141.1",
          "transcript_support_level": null,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 1117,
          "cds_start": 1476,
          "cds_end": null,
          "cds_length": 3354,
          "cdna_start": 1476,
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          "cdna_length": 3811,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1389C>T",
          "hgvs_p": "p.Ile463Ile",
          "transcript": "NM_001414030.1",
          "protein_id": "NP_001400959.1",
          "transcript_support_level": null,
          "aa_start": 463,
          "aa_end": null,
          "aa_length": 1112,
          "cds_start": 1389,
          "cds_end": null,
          "cds_length": 3339,
          "cdna_start": 1611,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
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          "exon_count": 26,
          "intron_rank": null,
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          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ile459Ile",
          "transcript": "NM_001414031.1",
          "protein_id": "NP_001400960.1",
          "transcript_support_level": null,
          "aa_start": 459,
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          "aa_length": 1108,
          "cds_start": 1377,
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        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1344C>T",
          "hgvs_p": "p.Ile448Ile",
          "transcript": "NM_001414032.1",
          "protein_id": "NP_001400961.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 1097,
          "cds_start": 1344,
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          "cdna_start": 1566,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
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          ],
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          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1281C>T",
          "hgvs_p": "p.Ile427Ile",
          "transcript": "NM_001414033.1",
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1464C>T",
          "hgvs_p": "p.Ile488Ile",
          "transcript": "NM_001414034.1",
          "protein_id": "NP_001400963.1",
          "transcript_support_level": null,
          "aa_start": 488,
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          "cds_start": 1464,
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        },
        {
          "aa_ref": "I",
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          "canonical": false,
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          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1185C>T",
          "hgvs_p": "p.Ile395Ile",
          "transcript": "NM_001144997.2",
          "protein_id": "NP_001138469.1",
          "transcript_support_level": null,
          "aa_start": 395,
          "aa_end": null,
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          "cdna_start": 1324,
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        },
        {
          "aa_ref": "I",
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          ],
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          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "ITGA7",
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        },
        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ITGA7",
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          "hgvs_c": "c.1137C>T",
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          "transcript": "NM_001367993.1",
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        },
        {
          "aa_ref": "I",
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          "consequences": [
            "synonymous_variant"
          ],
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          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "c.1125C>T",
          "hgvs_p": "p.Ile375Ile",
          "transcript": "NM_001414035.1",
          "protein_id": "NP_001400964.1",
          "transcript_support_level": null,
          "aa_start": 375,
          "aa_end": null,
          "aa_length": 1024,
          "cds_start": 1125,
          "cds_end": null,
          "cds_length": 3075,
          "cdna_start": 1438,
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          "cdna_length": 3878,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 23,
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3778,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITGA7",
          "gene_hgnc_id": 6143,
          "hgvs_c": "n.*1175C>T",
          "hgvs_p": null,
          "transcript": "ENST00000686981.1",
          "protein_id": "ENSP00000510795.1",
          "transcript_support_level": null,
          "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": 3880,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ITGA7",
      "gene_hgnc_id": 6143,
      "dbsnp": "rs202051829",
      "frequency_reference_population": 0.00036552697,
      "hom_count_reference_population": 1,
      "allele_count_reference_population": 590,
      "gnomad_exomes_af": 0.000386524,
      "gnomad_genomes_af": 0.000164083,
      "gnomad_exomes_ac": 565,
      "gnomad_genomes_ac": 25,
      "gnomad_exomes_homalt": 1,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7300000190734863,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.029999999329447746,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.73,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -2.705,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.03,
      "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,BS1",
      "acmg_by_gene": [
        {
          "score": -16,
          "benign_score": 16,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000257879.11",
          "gene_symbol": "ITGA7",
          "hgnc_id": 6143,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.1464C>T",
          "hgvs_p": "p.Ile488Ile"
        }
      ],
      "clinvar_disease": "Congenital muscular dystrophy due to integrin alpha-7 deficiency,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "not specified|Congenital muscular dystrophy due to integrin alpha-7 deficiency",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}