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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: 5-138933973-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=138933973&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 138933973,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "NM_001903.5",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2605T>C",
          "hgvs_p": "p.Leu869Leu",
          "transcript": "NM_001903.5",
          "protein_id": "NP_001894.2",
          "transcript_support_level": null,
          "aa_start": 869,
          "aa_end": null,
          "aa_length": 906,
          "cds_start": 2605,
          "cds_end": null,
          "cds_length": 2721,
          "cdna_start": 2693,
          "cdna_end": null,
          "cdna_length": 3754,
          "mane_select": "ENST00000302763.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2605T>C",
          "hgvs_p": "p.Leu869Leu",
          "transcript": "ENST00000302763.12",
          "protein_id": "ENSP00000304669.7",
          "transcript_support_level": 1,
          "aa_start": 869,
          "aa_end": null,
          "aa_length": 906,
          "cds_start": 2605,
          "cds_end": null,
          "cds_length": 2721,
          "cdna_start": 2693,
          "cdna_end": null,
          "cdna_length": 3754,
          "mane_select": "NM_001903.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "ENST00000540387.5",
          "protein_id": "ENSP00000438476.1",
          "transcript_support_level": 1,
          "aa_start": 499,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1495,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": 1629,
          "cdna_end": null,
          "cdna_length": 2684,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.*150T>C",
          "hgvs_p": null,
          "transcript": "ENST00000518825.5",
          "protein_id": "ENSP00000427821.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 841,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2526,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3536,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2605T>C",
          "hgvs_p": "p.Leu869Leu",
          "transcript": "NM_001323982.2",
          "protein_id": "NP_001310911.1",
          "transcript_support_level": null,
          "aa_start": 869,
          "aa_end": null,
          "aa_length": 906,
          "cds_start": 2605,
          "cds_end": null,
          "cds_length": 2721,
          "cdna_start": 3163,
          "cdna_end": null,
          "cdna_length": 4224,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2605T>C",
          "hgvs_p": "p.Leu869Leu",
          "transcript": "NM_001323983.1",
          "protein_id": "NP_001310912.1",
          "transcript_support_level": null,
          "aa_start": 869,
          "aa_end": null,
          "aa_length": 906,
          "cds_start": 2605,
          "cds_end": null,
          "cds_length": 2721,
          "cdna_start": 2884,
          "cdna_end": null,
          "cdna_length": 3945,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2605T>C",
          "hgvs_p": "p.Leu869Leu",
          "transcript": "NM_001323984.2",
          "protein_id": "NP_001310913.1",
          "transcript_support_level": null,
          "aa_start": 869,
          "aa_end": null,
          "aa_length": 906,
          "cds_start": 2605,
          "cds_end": null,
          "cds_length": 2721,
          "cdna_start": 2711,
          "cdna_end": null,
          "cdna_length": 3772,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2578T>C",
          "hgvs_p": "p.Leu860Leu",
          "transcript": "NM_001323985.2",
          "protein_id": "NP_001310914.1",
          "transcript_support_level": null,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 897,
          "cds_start": 2578,
          "cds_end": null,
          "cds_length": 2694,
          "cdna_start": 2666,
          "cdna_end": null,
          "cdna_length": 3727,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2512T>C",
          "hgvs_p": "p.Leu838Leu",
          "transcript": "NM_001323986.2",
          "protein_id": "NP_001310915.1",
          "transcript_support_level": null,
          "aa_start": 838,
          "aa_end": null,
          "aa_length": 875,
          "cds_start": 2512,
          "cds_end": null,
          "cds_length": 2628,
          "cdna_start": 2600,
          "cdna_end": null,
          "cdna_length": 3661,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2296T>C",
          "hgvs_p": "p.Leu766Leu",
          "transcript": "NM_001290309.3",
          "protein_id": "NP_001277238.1",
          "transcript_support_level": null,
          "aa_start": 766,
          "aa_end": null,
          "aa_length": 803,
          "cds_start": 2296,
          "cds_end": null,
          "cds_length": 2412,
          "cdna_start": 2497,
          "cdna_end": null,
          "cdna_length": 3558,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.2236T>C",
          "hgvs_p": "p.Leu746Leu",
          "transcript": "NM_001290310.3",
          "protein_id": "NP_001277239.1",
          "transcript_support_level": null,
          "aa_start": 746,
          "aa_end": null,
          "aa_length": 783,
          "cds_start": 2236,
          "cds_end": null,
          "cds_length": 2352,
          "cdna_start": 2530,
          "cdna_end": null,
          "cdna_length": 3591,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001290312.1",
          "protein_id": "NP_001277241.1",
          "transcript_support_level": null,
          "aa_start": 499,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1495,
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          "cds_length": 1611,
          "cdna_start": 2052,
          "cdna_end": null,
          "cdna_length": 3113,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323987.1",
          "protein_id": "NP_001310916.1",
          "transcript_support_level": null,
          "aa_start": 499,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1495,
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          "cdna_start": 1741,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323988.1",
          "protein_id": "NP_001310917.1",
          "transcript_support_level": null,
          "aa_start": 499,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1495,
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          "cdna_start": 1989,
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          "cdna_length": 3050,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 13,
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          "intron_rank": null,
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          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323989.1",
          "protein_id": "NP_001310918.1",
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          "aa_start": 499,
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          "cds_start": 1495,
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          "cdna_start": 1837,
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          "cdna_length": 2898,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323990.1",
          "protein_id": "NP_001310919.1",
          "transcript_support_level": null,
          "aa_start": 499,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1495,
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          "cdna_start": 2201,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323991.1",
          "protein_id": "NP_001310920.1",
          "transcript_support_level": null,
          "aa_start": 499,
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          "aa_length": 536,
          "cds_start": 1495,
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          "cdna_start": 2148,
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          "cdna_length": 3209,
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        },
        {
          "aa_ref": "L",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
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          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323992.1",
          "protein_id": "NP_001310921.1",
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        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
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          "exon_count": 15,
          "intron_rank": null,
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          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323993.1",
          "protein_id": "NP_001310922.1",
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.1495T>C",
          "hgvs_p": "p.Leu499Leu",
          "transcript": "NM_001323994.1",
          "protein_id": "NP_001310923.1",
          "transcript_support_level": null,
          "aa_start": 499,
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          "cds_start": 1495,
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          "cds_length": 1611,
          "cdna_start": 1750,
          "cdna_end": null,
          "cdna_length": 2811,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
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          "cds_length": 1416,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3333,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.*150T>C",
          "hgvs_p": null,
          "transcript": "NM_001324004.1",
          "protein_id": "NP_001310933.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 471,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1416,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2873,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "c.*150T>C",
          "hgvs_p": null,
          "transcript": "NM_001324005.1",
          "protein_id": "NP_001310934.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 471,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1416,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3408,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTNNA1",
          "gene_hgnc_id": 2509,
          "hgvs_c": "n.*2295T>C",
          "hgvs_p": null,
          "transcript": "ENST00000521724.5",
          "protein_id": "ENSP00000431033.1",
          "transcript_support_level": 2,
          "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": 2741,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CTNNA1",
      "gene_hgnc_id": 2509,
      "dbsnp": "rs756274664",
      "frequency_reference_population": 0.000018469293,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 27,
      "gnomad_exomes_af": 0.0000184693,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 27,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6000000238418579,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.6,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.1,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -17,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -17,
          "benign_score": 17,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_001903.5",
          "gene_symbol": "CTNNA1",
          "hgnc_id": 2509,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2605T>C",
          "hgvs_p": "p.Leu869Leu"
        }
      ],
      "clinvar_disease": "Hereditary cancer-predisposing syndrome,Hereditary diffuse gastric adenocarcinoma,not provided",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2 B:1",
      "phenotype_combined": "not provided|Hereditary cancer-predisposing syndrome|Hereditary diffuse gastric adenocarcinoma",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}