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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: 10-3138035-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=3138035&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 3138035,
      "ref": "T",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000224949.9",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.3110A>C",
          "hgvs_p": "p.Gln1037Pro",
          "transcript": "NM_014889.4",
          "protein_id": "NP_055704.2",
          "transcript_support_level": null,
          "aa_start": 1037,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": 3110,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": 3120,
          "cdna_end": null,
          "cdna_length": 3427,
          "mane_select": "ENST00000224949.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.3110A>C",
          "hgvs_p": "p.Gln1037Pro",
          "transcript": "ENST00000224949.9",
          "protein_id": "ENSP00000224949.4",
          "transcript_support_level": 1,
          "aa_start": 1037,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": 3110,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": 3120,
          "cdna_end": null,
          "cdna_length": 3427,
          "mane_select": "NM_014889.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.3113A>C",
          "hgvs_p": "p.Gln1038Pro",
          "transcript": "ENST00000380989.6",
          "protein_id": "ENSP00000370377.2",
          "transcript_support_level": 1,
          "aa_start": 1038,
          "aa_end": null,
          "aa_length": 1038,
          "cds_start": 3113,
          "cds_end": null,
          "cds_length": 3117,
          "cdna_start": 3182,
          "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.2933A>C",
          "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": "Q",
          "aa_alt": "P",
          "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.3113A>C",
          "hgvs_p": "p.Gln1038Pro",
          "transcript": "NM_001242307.2",
          "protein_id": "NP_001229236.1",
          "transcript_support_level": null,
          "aa_start": 1038,
          "aa_end": null,
          "aa_length": 1038,
          "cds_start": 3113,
          "cds_end": null,
          "cds_length": 3117,
          "cdna_start": 3123,
          "cdna_end": null,
          "cdna_length": 3430,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.3086A>C",
          "hgvs_p": "p.Gln1029Pro",
          "transcript": "NM_001347729.1",
          "protein_id": "NP_001334658.1",
          "transcript_support_level": null,
          "aa_start": 1029,
          "aa_end": null,
          "aa_length": 1029,
          "cds_start": 3086,
          "cds_end": null,
          "cds_length": 3090,
          "cdna_start": 3589,
          "cdna_end": null,
          "cdna_length": 3897,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.3062A>C",
          "hgvs_p": "p.Gln1021Pro",
          "transcript": "ENST00000678987.1",
          "protein_id": "ENSP00000504462.1",
          "transcript_support_level": null,
          "aa_start": 1021,
          "aa_end": null,
          "aa_length": 1021,
          "cds_start": 3062,
          "cds_end": null,
          "cds_length": 3066,
          "cdna_start": 3079,
          "cdna_end": null,
          "cdna_length": 3374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2987A>C",
          "hgvs_p": "p.Gln996Pro",
          "transcript": "ENST00000678441.1",
          "protein_id": "ENSP00000504785.1",
          "transcript_support_level": null,
          "aa_start": 996,
          "aa_end": null,
          "aa_length": 996,
          "cds_start": 2987,
          "cds_end": null,
          "cds_length": 2991,
          "cdna_start": 3005,
          "cdna_end": null,
          "cdna_length": 3294,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2984A>C",
          "hgvs_p": "p.Gln995Pro",
          "transcript": "ENST00000678370.1",
          "protein_id": "ENSP00000504540.1",
          "transcript_support_level": null,
          "aa_start": 995,
          "aa_end": null,
          "aa_length": 995,
          "cds_start": 2984,
          "cds_end": null,
          "cds_length": 2988,
          "cdna_start": 3018,
          "cdna_end": null,
          "cdna_length": 3307,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2975A>C",
          "hgvs_p": "p.Gln992Pro",
          "transcript": "ENST00000676953.1",
          "protein_id": "ENSP00000504468.1",
          "transcript_support_level": null,
          "aa_start": 992,
          "aa_end": null,
          "aa_length": 992,
          "cds_start": 2975,
          "cds_end": null,
          "cds_length": 2979,
          "cdna_start": 2982,
          "cdna_end": null,
          "cdna_length": 3277,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2912A>C",
          "hgvs_p": "p.Gln971Pro",
          "transcript": "NM_001347725.2",
          "protein_id": "NP_001334654.1",
          "transcript_support_level": null,
          "aa_start": 971,
          "aa_end": null,
          "aa_length": 971,
          "cds_start": 2912,
          "cds_end": null,
          "cds_length": 2916,
          "cdna_start": 2922,
          "cdna_end": null,
          "cdna_length": 3229,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2912A>C",
          "hgvs_p": "p.Gln971Pro",
          "transcript": "ENST00000678436.1",
          "protein_id": "ENSP00000503187.1",
          "transcript_support_level": null,
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          "aa_length": 971,
          "cds_start": 2912,
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          "cdna_start": 2947,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "Q",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
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          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2888A>C",
          "hgvs_p": "p.Gln963Pro",
          "transcript": "NM_001347730.1",
          "protein_id": "NP_001334659.1",
          "transcript_support_level": null,
          "aa_start": 963,
          "aa_end": null,
          "aa_length": 963,
          "cds_start": 2888,
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          "cdna_start": 3391,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2816A>C",
          "hgvs_p": "p.Gln939Pro",
          "transcript": "NM_001242309.1",
          "protein_id": "NP_001229238.1",
          "transcript_support_level": null,
          "aa_start": 939,
          "aa_end": null,
          "aa_length": 939,
          "cds_start": 2816,
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          "cds_length": 2820,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "canonical": false,
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2816A>C",
          "hgvs_p": "p.Gln939Pro",
          "transcript": "ENST00000451104.6",
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          "aa_start": 939,
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          "aa_length": 939,
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          "cdna_start": 2878,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.2495A>C",
          "hgvs_p": "p.Gln832Pro",
          "transcript": "NM_001347727.2",
          "protein_id": "NP_001334656.1",
          "transcript_support_level": null,
          "aa_start": 832,
          "aa_end": null,
          "aa_length": 832,
          "cds_start": 2495,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
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          "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.2495A>C",
          "hgvs_p": "p.Gln832Pro",
          "transcript": "ENST00000380994.6",
          "protein_id": "ENSP00000370382.2",
          "transcript_support_level": 5,
          "aa_start": 832,
          "aa_end": null,
          "aa_length": 832,
          "cds_start": 2495,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 25,
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          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2297A>C",
          "hgvs_p": "p.Gln766Pro",
          "transcript": "NM_001347726.2",
          "protein_id": "NP_001334655.1",
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "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.1805A>C",
          "hgvs_p": "p.Gln602Pro",
          "transcript": "NM_001347728.2",
          "protein_id": "NP_001334657.1",
          "transcript_support_level": null,
          "aa_start": 602,
          "aa_end": null,
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          "cds_length": 1809,
          "cdna_start": 3115,
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          "cdna_length": 3422,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "P",
          "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.1454A>C",
          "hgvs_p": "p.Gln485Pro",
          "transcript": "ENST00000678811.1",
          "protein_id": "ENSP00000504078.1",
          "transcript_support_level": null,
          "aa_start": 485,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 1454,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 1455,
          "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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      "acmg_by_gene": [
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            "BP4_Moderate"
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          "verdict": "Uncertain_significance",
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            "BP4_Moderate"
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          "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
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  ],
  "message": null
}