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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: 11-792570-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=792570&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 792570,
      "ref": "G",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "NM_001425334.1",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "NM_001191061.2",
          "protein_id": "NP_001177990.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 798,
          "cdna_end": null,
          "cdna_length": 2640,
          "mane_select": "ENST00000628067.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001191061.2"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000628067.3",
          "protein_id": "ENSP00000486058.1",
          "transcript_support_level": 1,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 798,
          "cdna_end": null,
          "cdna_length": 2640,
          "mane_select": "NM_001191061.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000628067.3"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000320230.9",
          "protein_id": "ENSP00000322020.5",
          "transcript_support_level": 1,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 954,
          "cdna_end": null,
          "cdna_length": 2796,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000320230.9"
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "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": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.562C>G",
          "hgvs_p": "p.Arg188Gly",
          "transcript": "ENST00000937625.1",
          "protein_id": "ENSP00000607684.1",
          "transcript_support_level": null,
          "aa_start": 188,
          "aa_end": null,
          "aa_length": 303,
          "cds_start": 562,
          "cds_end": null,
          "cds_length": 912,
          "cdna_start": 772,
          "cdna_end": null,
          "cdna_length": 2561,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000937625.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.645C>G",
          "hgvs_p": "p.Leu215Leu",
          "transcript": "NM_001425334.1",
          "protein_id": "NP_001412263.1",
          "transcript_support_level": null,
          "aa_start": 215,
          "aa_end": null,
          "aa_length": 348,
          "cds_start": 645,
          "cds_end": null,
          "cds_length": 1047,
          "cdna_start": 873,
          "cdna_end": null,
          "cdna_length": 2715,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001425334.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.645C>G",
          "hgvs_p": "p.Leu215Leu",
          "transcript": "ENST00000860087.1",
          "protein_id": "ENSP00000530146.1",
          "transcript_support_level": null,
          "aa_start": 215,
          "aa_end": null,
          "aa_length": 348,
          "cds_start": 645,
          "cds_end": null,
          "cds_length": 1047,
          "cdna_start": 859,
          "cdna_end": null,
          "cdna_length": 2697,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860087.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.609C>G",
          "hgvs_p": "p.Leu203Leu",
          "transcript": "NM_001425335.1",
          "protein_id": "NP_001412264.1",
          "transcript_support_level": null,
          "aa_start": 203,
          "aa_end": null,
          "aa_length": 336,
          "cds_start": 609,
          "cds_end": null,
          "cds_length": 1011,
          "cdna_start": 837,
          "cdna_end": null,
          "cdna_length": 2679,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001425335.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.585C>G",
          "hgvs_p": "p.Leu195Leu",
          "transcript": "NM_001425336.1",
          "protein_id": "NP_001412265.1",
          "transcript_support_level": null,
          "aa_start": 195,
          "aa_end": null,
          "aa_length": 328,
          "cds_start": 585,
          "cds_end": null,
          "cds_length": 987,
          "cdna_start": 813,
          "cdna_end": null,
          "cdna_length": 2655,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001425336.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000948531.1",
          "protein_id": "ENSP00000618590.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 327,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 984,
          "cdna_start": 762,
          "cdna_end": null,
          "cdna_length": 2613,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000948531.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "NM_001191060.2",
          "protein_id": "NP_001177989.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 1120,
          "cdna_end": null,
          "cdna_length": 2962,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001191060.2"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "NM_001425337.1",
          "protein_id": "NP_001412266.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 826,
          "cdna_end": null,
          "cdna_length": 2668,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001425337.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "NM_001425338.1",
          "protein_id": "NP_001412267.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 1123,
          "cdna_end": null,
          "cdna_length": 2965,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001425338.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "NM_001425339.1",
          "protein_id": "NP_001412268.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 793,
          "cdna_end": null,
          "cdna_length": 2635,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001425339.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "NM_024698.6",
          "protein_id": "NP_078974.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 929,
          "cdna_end": null,
          "cdna_length": 2771,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_024698.6"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000531214.5",
          "protein_id": "ENSP00000437236.1",
          "transcript_support_level": 2,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 1117,
          "cdna_end": null,
          "cdna_length": 1790,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000531214.5"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000860084.1",
          "protein_id": "ENSP00000530143.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 828,
          "cdna_end": null,
          "cdna_length": 2670,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860084.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000860086.1",
          "protein_id": "ENSP00000530145.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 896,
          "cdna_end": null,
          "cdna_length": 2738,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000860086.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000860088.1",
          "protein_id": "ENSP00000530147.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 977,
          "cdna_end": null,
          "cdna_length": 2806,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860088.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000860089.1",
          "protein_id": "ENSP00000530148.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 972,
          "cdna_start": 1096,
          "cdna_end": null,
          "cdna_length": 2937,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860089.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "c.570C>G",
          "hgvs_p": "p.Leu190Leu",
          "transcript": "ENST00000860091.1",
          "protein_id": "ENSP00000530150.1",
          "transcript_support_level": null,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 323,
          "cds_start": 570,
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          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC25A22",
          "gene_hgnc_id": 19954,
          "hgvs_c": "n.*356C>G",
          "hgvs_p": null,
          "transcript": "ENST00000531514.5",
          "protein_id": "ENSP00000433780.2",
          "transcript_support_level": 4,
          "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": 641,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000531514.5"
        }
      ],
      "gene_symbol": "SLC25A22",
      "gene_hgnc_id": 19954,
      "dbsnp": "rs145322467",
      "frequency_reference_population": 0.0000018611853,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 3,
      "gnomad_exomes_af": 6.84969e-7,
      "gnomad_genomes_af": 0.0000131617,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6499999761581421,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.65,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.382,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001425334.1",
          "gene_symbol": "SLC25A22",
          "hgnc_id": 19954,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.645C>G",
          "hgvs_p": "p.Leu215Leu"
        }
      ],
      "clinvar_disease": "Developmental and epileptic encephalopathy",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Developmental and epileptic encephalopathy",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}
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