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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: 10-3138096-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=3138096&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 3138096,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000224949.9",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.3049G>T",
          "hgvs_p": "p.Gly1017Cys",
          "transcript": "NM_014889.4",
          "protein_id": "NP_055704.2",
          "transcript_support_level": null,
          "aa_start": 1017,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": 3049,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": 3059,
          "cdna_end": null,
          "cdna_length": 3427,
          "mane_select": "ENST00000224949.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.3049G>T",
          "hgvs_p": "p.Gly1017Cys",
          "transcript": "ENST00000224949.9",
          "protein_id": "ENSP00000224949.4",
          "transcript_support_level": 1,
          "aa_start": 1017,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": 3049,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": 3059,
          "cdna_end": null,
          "cdna_length": 3427,
          "mane_select": "NM_014889.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.3052G>T",
          "hgvs_p": "p.Gly1018Cys",
          "transcript": "ENST00000380989.6",
          "protein_id": "ENSP00000370377.2",
          "transcript_support_level": 1,
          "aa_start": 1018,
          "aa_end": null,
          "aa_length": 1038,
          "cds_start": 3052,
          "cds_end": null,
          "cds_length": 3117,
          "cdna_start": 3121,
          "cdna_end": null,
          "cdna_length": 3487,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "n.2872G>T",
          "hgvs_p": null,
          "transcript": "ENST00000464395.1",
          "protein_id": null,
          "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": 3240,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.3052G>T",
          "hgvs_p": "p.Gly1018Cys",
          "transcript": "NM_001242307.2",
          "protein_id": "NP_001229236.1",
          "transcript_support_level": null,
          "aa_start": 1018,
          "aa_end": null,
          "aa_length": 1038,
          "cds_start": 3052,
          "cds_end": null,
          "cds_length": 3117,
          "cdna_start": 3062,
          "cdna_end": null,
          "cdna_length": 3430,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.3025G>T",
          "hgvs_p": "p.Gly1009Cys",
          "transcript": "NM_001347729.1",
          "protein_id": "NP_001334658.1",
          "transcript_support_level": null,
          "aa_start": 1009,
          "aa_end": null,
          "aa_length": 1029,
          "cds_start": 3025,
          "cds_end": null,
          "cds_length": 3090,
          "cdna_start": 3528,
          "cdna_end": null,
          "cdna_length": 3897,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.3001G>T",
          "hgvs_p": "p.Gly1001Cys",
          "transcript": "ENST00000678987.1",
          "protein_id": "ENSP00000504462.1",
          "transcript_support_level": null,
          "aa_start": 1001,
          "aa_end": null,
          "aa_length": 1021,
          "cds_start": 3001,
          "cds_end": null,
          "cds_length": 3066,
          "cdna_start": 3018,
          "cdna_end": null,
          "cdna_length": 3374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2926G>T",
          "hgvs_p": "p.Gly976Cys",
          "transcript": "ENST00000678441.1",
          "protein_id": "ENSP00000504785.1",
          "transcript_support_level": null,
          "aa_start": 976,
          "aa_end": null,
          "aa_length": 996,
          "cds_start": 2926,
          "cds_end": null,
          "cds_length": 2991,
          "cdna_start": 2944,
          "cdna_end": null,
          "cdna_length": 3294,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2923G>T",
          "hgvs_p": "p.Gly975Cys",
          "transcript": "ENST00000678370.1",
          "protein_id": "ENSP00000504540.1",
          "transcript_support_level": null,
          "aa_start": 975,
          "aa_end": null,
          "aa_length": 995,
          "cds_start": 2923,
          "cds_end": null,
          "cds_length": 2988,
          "cdna_start": 2957,
          "cdna_end": null,
          "cdna_length": 3307,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2914G>T",
          "hgvs_p": "p.Gly972Cys",
          "transcript": "ENST00000676953.1",
          "protein_id": "ENSP00000504468.1",
          "transcript_support_level": null,
          "aa_start": 972,
          "aa_end": null,
          "aa_length": 992,
          "cds_start": 2914,
          "cds_end": null,
          "cds_length": 2979,
          "cdna_start": 2921,
          "cdna_end": null,
          "cdna_length": 3277,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2851G>T",
          "hgvs_p": "p.Gly951Cys",
          "transcript": "NM_001347725.2",
          "protein_id": "NP_001334654.1",
          "transcript_support_level": null,
          "aa_start": 951,
          "aa_end": null,
          "aa_length": 971,
          "cds_start": 2851,
          "cds_end": null,
          "cds_length": 2916,
          "cdna_start": 2861,
          "cdna_end": null,
          "cdna_length": 3229,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2851G>T",
          "hgvs_p": "p.Gly951Cys",
          "transcript": "ENST00000678436.1",
          "protein_id": "ENSP00000503187.1",
          "transcript_support_level": null,
          "aa_start": 951,
          "aa_end": null,
          "aa_length": 971,
          "cds_start": 2851,
          "cds_end": null,
          "cds_length": 2916,
          "cdna_start": 2886,
          "cdna_end": null,
          "cdna_length": 3242,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2827G>T",
          "hgvs_p": "p.Gly943Cys",
          "transcript": "NM_001347730.1",
          "protein_id": "NP_001334659.1",
          "transcript_support_level": null,
          "aa_start": 943,
          "aa_end": null,
          "aa_length": 963,
          "cds_start": 2827,
          "cds_end": null,
          "cds_length": 2892,
          "cdna_start": 3330,
          "cdna_end": null,
          "cdna_length": 3699,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2755G>T",
          "hgvs_p": "p.Gly919Cys",
          "transcript": "NM_001242309.1",
          "protein_id": "NP_001229238.1",
          "transcript_support_level": null,
          "aa_start": 919,
          "aa_end": null,
          "aa_length": 939,
          "cds_start": 2755,
          "cds_end": null,
          "cds_length": 2820,
          "cdna_start": 2817,
          "cdna_end": null,
          "cdna_length": 3185,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2755G>T",
          "hgvs_p": "p.Gly919Cys",
          "transcript": "ENST00000451104.6",
          "protein_id": "ENSP00000401201.2",
          "transcript_support_level": 2,
          "aa_start": 919,
          "aa_end": null,
          "aa_length": 939,
          "cds_start": 2755,
          "cds_end": null,
          "cds_length": 2820,
          "cdna_start": 2817,
          "cdna_end": null,
          "cdna_length": 3183,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2434G>T",
          "hgvs_p": "p.Gly812Cys",
          "transcript": "NM_001347727.2",
          "protein_id": "NP_001334656.1",
          "transcript_support_level": null,
          "aa_start": 812,
          "aa_end": null,
          "aa_length": 832,
          "cds_start": 2434,
          "cds_end": null,
          "cds_length": 2499,
          "cdna_start": 3015,
          "cdna_end": null,
          "cdna_length": 3383,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2434G>T",
          "hgvs_p": "p.Gly812Cys",
          "transcript": "ENST00000380994.6",
          "protein_id": "ENSP00000370382.2",
          "transcript_support_level": 5,
          "aa_start": 812,
          "aa_end": null,
          "aa_length": 832,
          "cds_start": 2434,
          "cds_end": null,
          "cds_length": 2499,
          "cdna_start": 2917,
          "cdna_end": null,
          "cdna_length": 3274,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2236G>T",
          "hgvs_p": "p.Gly746Cys",
          "transcript": "NM_001347726.2",
          "protein_id": "NP_001334655.1",
          "transcript_support_level": null,
          "aa_start": 746,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 2236,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 2817,
          "cdna_end": null,
          "cdna_length": 3185,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.1744G>T",
          "hgvs_p": "p.Gly582Cys",
          "transcript": "NM_001347728.2",
          "protein_id": "NP_001334657.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 602,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 1809,
          "cdna_start": 3054,
          "cdna_end": null,
          "cdna_length": 3422,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "C",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.1393G>T",
          "hgvs_p": "p.Gly465Cys",
          "transcript": "ENST00000678811.1",
          "protein_id": "ENSP00000504078.1",
          "transcript_support_level": null,
          "aa_start": 465,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 1393,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 1394,
          "cdna_end": null,
          "cdna_length": 1762,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
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      "frequency_reference_population": 6.8583154e-7,
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      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.85832e-7,
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      "revel_prediction": "Uncertain_significance",
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      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.1,
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      "spliceai_max_score": 0,
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      "acmg_score": 3,
      "acmg_classification": "Uncertain_significance",
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      "acmg_by_gene": [
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            "PP3"
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          "verdict": "Uncertain_significance",
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        {
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            "PP3"
          ],
          "verdict": "Uncertain_significance",
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          "effects": [
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          ],
          "inheritance_mode": "",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}