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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: X-48981803-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=48981803&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 48981803,
      "ref": "C",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "NM_020137.5",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "NM_020137.5",
          "protein_id": "NP_064522.4",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 841,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2526,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000376423.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_020137.5"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000376423.8",
          "protein_id": "ENSP00000365606.5",
          "transcript_support_level": 1,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 841,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2526,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_020137.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000376423.8"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1744G>A",
          "hgvs_p": "p.Glu582Lys",
          "transcript": "ENST00000900849.1",
          "protein_id": "ENSP00000570908.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 898,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 2697,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000900849.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1744G>A",
          "hgvs_p": "p.Glu582Lys",
          "transcript": "ENST00000946827.1",
          "protein_id": "ENSP00000616886.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 897,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 2694,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000946827.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1798G>A",
          "hgvs_p": "p.Glu600Lys",
          "transcript": "ENST00000703962.1",
          "protein_id": "ENSP00000515589.1",
          "transcript_support_level": null,
          "aa_start": 600,
          "aa_end": null,
          "aa_length": 884,
          "cds_start": 1798,
          "cds_end": null,
          "cds_length": 2655,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703962.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1774G>A",
          "hgvs_p": "p.Glu592Lys",
          "transcript": "ENST00000704020.1",
          "protein_id": "ENSP00000515632.1",
          "transcript_support_level": null,
          "aa_start": 592,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": 1774,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000704020.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000703932.1",
          "protein_id": "ENSP00000515566.1",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 873,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2622,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703932.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000704095.1",
          "protein_id": "ENSP00000515690.1",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 872,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2619,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000704095.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000900846.1",
          "protein_id": "ENSP00000570905.1",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 867,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2604,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000900846.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1744G>A",
          "hgvs_p": "p.Glu582Lys",
          "transcript": "ENST00000703876.1",
          "protein_id": "ENSP00000515519.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 866,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 2601,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703876.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1732G>A",
          "hgvs_p": "p.Glu578Lys",
          "transcript": "ENST00000704045.1",
          "protein_id": "ENSP00000515648.1",
          "transcript_support_level": null,
          "aa_start": 578,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 1732,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000704045.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1744G>A",
          "hgvs_p": "p.Glu582Lys",
          "transcript": "ENST00000900847.1",
          "protein_id": "ENSP00000570906.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 860,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 2583,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000900847.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1699G>A",
          "hgvs_p": "p.Glu567Lys",
          "transcript": "ENST00000703927.1",
          "protein_id": "ENSP00000515561.1",
          "transcript_support_level": null,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 1699,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703927.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1702G>A",
          "hgvs_p": "p.Glu568Lys",
          "transcript": "ENST00000704267.1",
          "protein_id": "ENSP00000515807.1",
          "transcript_support_level": null,
          "aa_start": 568,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 1702,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000704267.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000900851.1",
          "protein_id": "ENSP00000570910.1",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 848,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2547,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000900851.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000900845.1",
          "protein_id": "ENSP00000570904.1",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 846,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2541,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000900845.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1699G>A",
          "hgvs_p": "p.Glu567Lys",
          "transcript": "ENST00000946828.1",
          "protein_id": "ENSP00000616887.1",
          "transcript_support_level": null,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 845,
          "cds_start": 1699,
          "cds_end": null,
          "cds_length": 2538,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000946828.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1675G>A",
          "hgvs_p": "p.Glu559Lys",
          "transcript": "ENST00000937301.1",
          "protein_id": "ENSP00000607360.1",
          "transcript_support_level": null,
          "aa_start": 559,
          "aa_end": null,
          "aa_length": 843,
          "cds_start": 1675,
          "cds_end": null,
          "cds_length": 2532,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000937301.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys",
          "transcript": "ENST00000704106.1",
          "protein_id": "ENSP00000515699.1",
          "transcript_support_level": null,
          "aa_start": 557,
          "aa_end": null,
          "aa_length": 840,
          "cds_start": 1669,
          "cds_end": null,
          "cds_length": 2523,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000704106.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GRIPAP1",
          "gene_hgnc_id": 18706,
          "hgvs_c": "c.1666G>A",
          "hgvs_p": "p.Glu556Lys",
          "transcript": "ENST00000946831.1",
          "protein_id": "ENSP00000616890.1",
          "transcript_support_level": null,
          "aa_start": 556,
          "aa_end": null,
          "aa_length": 840,
          "cds_start": 1666,
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      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.1,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0989,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.29,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.646,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "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": -7,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6,BS2",
      "acmg_by_gene": [
        {
          "score": -7,
          "benign_score": 7,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_020137.5",
          "gene_symbol": "GRIPAP1",
          "hgnc_id": 18706,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.1669G>A",
          "hgvs_p": "p.Glu557Lys"
        }
      ],
      "clinvar_disease": "Seizure,not specified",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:1",
      "phenotype_combined": "Seizure|not specified",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}