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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: 7-114629915-GCAACAACAACAA-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=114629915&ref=GCAACAACAACAA&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 114629915,
      "ref": "GCAACAACAACAA",
      "alt": "G",
      "effect": "disruptive_inframe_deletion",
      "transcript": "ENST00000350908.9",
      "consequences": [
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "NM_014491.4",
          "protein_id": "NP_055306.1",
          "transcript_support_level": null,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 715,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 2148,
          "cdna_start": 1069,
          "cdna_end": null,
          "cdna_length": 6543,
          "mane_select": "ENST00000350908.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "ENST00000350908.9",
          "protein_id": "ENSP00000265436.7",
          "transcript_support_level": 1,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 715,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 2148,
          "cdna_start": 1069,
          "cdna_end": null,
          "cdna_length": 6543,
          "mane_select": "NM_014491.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.588_599delACAACAACAACA",
          "hgvs_p": "p.Gln197_Gln200del",
          "transcript": "ENST00000408937.7",
          "protein_id": "ENSP00000386200.3",
          "transcript_support_level": 1,
          "aa_start": 196,
          "aa_end": null,
          "aa_length": 740,
          "cds_start": 588,
          "cds_end": null,
          "cds_length": 2223,
          "cdna_start": 962,
          "cdna_end": null,
          "cdna_length": 6443,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.585_596delACAACAACAACA",
          "hgvs_p": "p.Gln196_Gln199del",
          "transcript": "ENST00000390668.3",
          "protein_id": "ENSP00000375084.3",
          "transcript_support_level": 1,
          "aa_start": 195,
          "aa_end": null,
          "aa_length": 456,
          "cds_start": 585,
          "cds_end": null,
          "cds_length": 1371,
          "cdna_start": 585,
          "cdna_end": null,
          "cdna_length": 1472,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "ENST00000360232.8",
          "protein_id": "ENSP00000353367.4",
          "transcript_support_level": 1,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 432,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 1299,
          "cdna_start": 525,
          "cdna_end": null,
          "cdna_length": 1412,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "ENST00000378237.7",
          "protein_id": "ENSP00000367482.3",
          "transcript_support_level": 1,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 365,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 1098,
          "cdna_start": 565,
          "cdna_end": null,
          "cdna_length": 2187,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "n.*307_*318delACAACAACAACA",
          "hgvs_p": null,
          "transcript": "ENST00000393489.8",
          "protein_id": "ENSP00000377129.4",
          "transcript_support_level": 1,
          "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": 2285,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "n.*700_*711delACAACAACAACA",
          "hgvs_p": null,
          "transcript": "ENST00000440349.5",
          "protein_id": "ENSP00000395552.1",
          "transcript_support_level": 1,
          "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": 1509,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "n.*307_*318delACAACAACAACA",
          "hgvs_p": null,
          "transcript": "ENST00000393489.8",
          "protein_id": "ENSP00000377129.4",
          "transcript_support_level": 1,
          "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": 2285,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "n.*700_*711delACAACAACAACA",
          "hgvs_p": null,
          "transcript": "ENST00000440349.5",
          "protein_id": "ENSP00000395552.1",
          "transcript_support_level": 1,
          "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": 1509,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.639_650delACAACAACAACA",
          "hgvs_p": "p.Gln214_Gln217del",
          "transcript": "ENST00000703616.1",
          "protein_id": "ENSP00000515400.1",
          "transcript_support_level": null,
          "aa_start": 213,
          "aa_end": null,
          "aa_length": 757,
          "cds_start": 639,
          "cds_end": null,
          "cds_length": 2274,
          "cdna_start": 1073,
          "cdna_end": null,
          "cdna_length": 4587,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.588_599delACAACAACAACA",
          "hgvs_p": "p.Gln197_Gln200del",
          "transcript": "NM_148898.4",
          "protein_id": "NP_683696.2",
          "transcript_support_level": null,
          "aa_start": 196,
          "aa_end": null,
          "aa_length": 740,
          "cds_start": 588,
          "cds_end": null,
          "cds_length": 2223,
          "cdna_start": 1144,
          "cdna_end": null,
          "cdna_length": 6618,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.564_575delACAACAACAACA",
          "hgvs_p": "p.Gln189_Gln192del",
          "transcript": "NM_148900.4",
          "protein_id": "NP_683698.2",
          "transcript_support_level": null,
          "aa_start": 188,
          "aa_end": null,
          "aa_length": 732,
          "cds_start": 564,
          "cds_end": null,
          "cds_length": 2199,
          "cdna_start": 1120,
          "cdna_end": null,
          "cdna_length": 6594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.564_575delACAACAACAACA",
          "hgvs_p": "p.Gln189_Gln192del",
          "transcript": "ENST00000403559.9",
          "protein_id": "ENSP00000385069.4",
          "transcript_support_level": 2,
          "aa_start": 188,
          "aa_end": null,
          "aa_length": 732,
          "cds_start": 564,
          "cds_end": null,
          "cds_length": 2199,
          "cdna_start": 818,
          "cdna_end": null,
          "cdna_length": 2807,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.564_575delACAACAACAACA",
          "hgvs_p": "p.Gln189_Gln192del",
          "transcript": "ENST00000703613.1",
          "protein_id": "ENSP00000515397.1",
          "transcript_support_level": null,
          "aa_start": 188,
          "aa_end": null,
          "aa_length": 732,
          "cds_start": 564,
          "cds_end": null,
          "cds_length": 2199,
          "cdna_start": 1036,
          "cdna_end": null,
          "cdna_length": 2763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "ENST00000635638.1",
          "protein_id": "ENSP00000489073.1",
          "transcript_support_level": 5,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 716,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 2151,
          "cdna_start": 851,
          "cdna_end": null,
          "cdna_length": 2598,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "ENST00000393494.6",
          "protein_id": "ENSP00000377132.2",
          "transcript_support_level": 5,
          "aa_start": 171,
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          "aa_length": 715,
          "cds_start": 513,
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          "cds_length": 2148,
          "cdna_start": 792,
          "cdna_end": null,
          "cdna_length": 2664,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "ENST00000703614.1",
          "protein_id": "ENSP00000515398.1",
          "transcript_support_level": null,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 715,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 2148,
          "cdna_start": 867,
          "cdna_end": null,
          "cdna_length": 2597,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del",
          "transcript": "NM_001172766.3",
          "protein_id": "NP_001166237.1",
          "transcript_support_level": null,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 714,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 2145,
          "cdna_start": 1069,
          "cdna_end": null,
          "cdna_length": 6540,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FOXP2",
          "gene_hgnc_id": 13875,
          "hgvs_c": "c.504_515delACAACAACAACA",
          "hgvs_p": "p.Gln169_Gln172del",
          "transcript": "ENST00000635534.1",
          "protein_id": "ENSP00000489229.1",
          "transcript_support_level": 5,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 504,
          "cds_end": null,
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      "phylop100way_score": 6.163,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -1,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP3",
      "acmg_by_gene": [
        {
          "score": -1,
          "benign_score": 1,
          "pathogenic_score": 0,
          "criteria": [
            "BP3"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000350908.9",
          "gene_symbol": "FOXP2",
          "hgnc_id": 13875,
          "effects": [
            "disruptive_inframe_deletion"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.513_524delACAACAACAACA",
          "hgvs_p": "p.Gln172_Gln175del"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}