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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 7-5997349-GG-CT (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=5997349&ref=GG&alt=CT&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 5997349,
      "ref": "GG",
      "alt": "CT",
      "effect": "stop_gained",
      "transcript": "ENST00000265849.12",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "NM_000535.7",
          "protein_id": "NP_000526.2",
          "transcript_support_level": null,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 779,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": 810,
          "cdna_end": null,
          "cdna_length": 5093,
          "mane_select": "ENST00000265849.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "ENST00000265849.12",
          "protein_id": "ENSP00000265849.7",
          "transcript_support_level": 1,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 779,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": 810,
          "cdna_end": null,
          "cdna_length": 5093,
          "mane_select": "NM_000535.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "ENST00000382321.5",
          "protein_id": "ENSP00000371758.4",
          "transcript_support_level": 1,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 461,
          "cds_start": 779,
          "cds_end": null,
          "cds_length": 1386,
          "cdna_start": 780,
          "cdna_end": null,
          "cdna_length": 1386,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.779_780delCCinsAG",
          "hgvs_p": null,
          "transcript": "ENST00000406569.8",
          "protein_id": "ENSP00000514464.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2101,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.62+8643_62+8644delCCinsAG",
          "hgvs_p": null,
          "transcript": "ENST00000469652.1",
          "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": 93,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.965_966delCCinsAG",
          "hgvs_p": "p.Ser322*",
          "transcript": "NM_001406866.1",
          "protein_id": "NP_001393795.1",
          "transcript_support_level": null,
          "aa_start": 322,
          "aa_end": null,
          "aa_length": 924,
          "cds_start": 965,
          "cds_end": null,
          "cds_length": 2775,
          "cdna_start": 996,
          "cdna_end": null,
          "cdna_length": 5279,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.965_966delCCinsAG",
          "hgvs_p": "p.Ser322*",
          "transcript": "ENST00000699839.1",
          "protein_id": "ENSP00000514637.1",
          "transcript_support_level": null,
          "aa_start": 322,
          "aa_end": null,
          "aa_length": 924,
          "cds_start": 965,
          "cds_end": null,
          "cds_length": 2775,
          "cdna_start": 1031,
          "cdna_end": null,
          "cdna_length": 3597,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "NM_001322014.2",
          "protein_id": "NP_001308943.1",
          "transcript_support_level": null,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 873,
          "cds_start": 779,
          "cds_end": null,
          "cds_length": 2622,
          "cdna_start": 810,
          "cdna_end": null,
          "cdna_length": 5126,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "ENST00000699766.1",
          "protein_id": "ENSP00000514574.1",
          "transcript_support_level": null,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 873,
          "cds_start": 779,
          "cds_end": null,
          "cds_length": 2622,
          "cdna_start": 883,
          "cdna_end": null,
          "cdna_length": 5167,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.803_804delCCinsAG",
          "hgvs_p": "p.Ser268*",
          "transcript": "NM_001406868.1",
          "protein_id": "NP_001393797.1",
          "transcript_support_level": null,
          "aa_start": 268,
          "aa_end": null,
          "aa_length": 870,
          "cds_start": 803,
          "cds_end": null,
          "cds_length": 2613,
          "cdna_start": 834,
          "cdna_end": null,
          "cdna_length": 5117,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.776_777delCCinsAG",
          "hgvs_p": "p.Ser259*",
          "transcript": "ENST00000699840.2",
          "protein_id": "ENSP00000514638.2",
          "transcript_support_level": null,
          "aa_start": 259,
          "aa_end": null,
          "aa_length": 861,
          "cds_start": 776,
          "cds_end": null,
          "cds_length": 2586,
          "cdna_start": 845,
          "cdna_end": null,
          "cdna_length": 2812,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.671_672delCCinsAG",
          "hgvs_p": "p.Ser224*",
          "transcript": "NM_001406869.1",
          "protein_id": "NP_001393798.1",
          "transcript_support_level": null,
          "aa_start": 224,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 671,
          "cds_end": null,
          "cds_length": 2481,
          "cdna_start": 702,
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          "cdna_length": 4985,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.671_672delCCinsAG",
          "hgvs_p": "p.Ser224*",
          "transcript": "ENST00000699930.2",
          "protein_id": "ENSP00000514695.2",
          "transcript_support_level": null,
          "aa_start": 224,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 671,
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          "cdna_start": 752,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "NM_001406870.1",
          "protein_id": "NP_001393799.1",
          "transcript_support_level": null,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 821,
          "cds_start": 779,
          "cds_end": null,
          "cds_length": 2466,
          "cdna_start": 810,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "NM_001406871.1",
          "protein_id": "NP_001393800.1",
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          "cdna_start": 810,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "ENST00000699768.1",
          "protein_id": "ENSP00000514576.1",
          "transcript_support_level": null,
          "aa_start": 260,
          "aa_end": null,
          "aa_length": 814,
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          "cdna_start": 883,
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          "cdna_length": 4990,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "NM_001322006.2",
          "protein_id": "NP_001308935.1",
          "transcript_support_level": null,
          "aa_start": 260,
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          "aa_length": 810,
          "cds_start": 779,
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          "cds_length": 2433,
          "cdna_start": 810,
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          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "ENST00000699752.1",
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          "biotype": null,
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        },
        {
          "aa_ref": "S",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*",
          "transcript": "NM_001406872.1",
          "protein_id": "NP_001393801.1",
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          "cds_start": 779,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.611_612delCCinsAG",
          "hgvs_p": "p.Ser204*",
          "transcript": "NM_001406874.1",
          "protein_id": "NP_001393803.1",
          "transcript_support_level": null,
          "aa_start": 204,
          "aa_end": null,
          "aa_length": 806,
          "cds_start": 611,
          "cds_end": null,
          "cds_length": 2421,
          "cdna_start": 642,
          "cdna_end": null,
          "cdna_length": 4925,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
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          "exon_count": 10,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.706-1717_706-1716delCCinsAG",
          "hgvs_p": null,
          "transcript": "ENST00000699953.1",
          "protein_id": "ENSP00000514708.1",
          "transcript_support_level": null,
          "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": 1806,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.*105-1717_*105-1716delCCinsAG",
          "hgvs_p": null,
          "transcript": "ENST00000699954.1",
          "protein_id": "ENSP00000514709.1",
          "transcript_support_level": null,
          "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": 1754,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-55_-54delCCinsAG",
          "hgvs_p": null,
          "transcript": "XM_047420486.1",
          "protein_id": "XP_047276442.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4180,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "PMS2",
      "gene_hgnc_id": 9122,
      "dbsnp": "rs730881920",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 0.588,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 10,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 10,
          "benign_score": 0,
          "pathogenic_score": 10,
          "criteria": [
            "PVS1",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000265849.12",
          "gene_symbol": "PMS2",
          "hgnc_id": 9122,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.779_780delCCinsAG",
          "hgvs_p": "p.Ser260*"
        }
      ],
      "clinvar_disease": "Hereditary nonpolyposis colorectal neoplasms",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "Hereditary nonpolyposis colorectal neoplasms",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}