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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: 7-6009009-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=6009009&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 6009009,
      "ref": "G",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "NM_000535.7",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.11C>T",
          "hgvs_p": "p.Ala4Val",
          "transcript": "NM_000535.7",
          "protein_id": "NP_000526.2",
          "transcript_support_level": null,
          "aa_start": 4,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 11,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": 41,
          "cdna_end": null,
          "cdna_length": 5093,
          "mane_select": "ENST00000265849.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "V",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.11C>T",
          "hgvs_p": "p.Ala4Val",
          "transcript": "ENST00000265849.12",
          "protein_id": "ENSP00000265849.7",
          "transcript_support_level": 1,
          "aa_start": 4,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 11,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": 41,
          "cdna_end": null,
          "cdna_length": 5093,
          "mane_select": "NM_000535.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.11C>T",
          "hgvs_p": "p.Ala4Val",
          "transcript": "ENST00000382321.5",
          "protein_id": "ENSP00000371758.4",
          "transcript_support_level": 1,
          "aa_start": 4,
          "aa_end": null,
          "aa_length": 461,
          "cds_start": 11,
          "cds_end": null,
          "cds_length": 1386,
          "cdna_start": 11,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.11C>T",
          "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": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.11C>T",
          "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": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-664C>T",
          "hgvs_p": null,
          "transcript": "NM_001406875.1",
          "protein_id": "NP_001393804.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 770,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2313,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5491,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-205C>T",
          "hgvs_p": null,
          "transcript": "NM_001406876.1",
          "protein_id": "NP_001393805.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 767,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2304,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5023,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-469C>T",
          "hgvs_p": null,
          "transcript": "NM_001322015.2",
          "protein_id": "NP_001308944.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 759,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2280,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5263,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-831C>T",
          "hgvs_p": null,
          "transcript": "NM_001406877.1",
          "protein_id": "NP_001393806.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 759,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2280,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5625,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-474C>T",
          "hgvs_p": null,
          "transcript": "NM_001406878.1",
          "protein_id": "NP_001393807.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 759,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2280,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5268,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-334C>T",
          "hgvs_p": null,
          "transcript": "NM_001406879.1",
          "protein_id": "NP_001393808.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 759,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2280,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5128,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-421C>T",
          "hgvs_p": null,
          "transcript": "NM_001406880.1",
          "protein_id": "NP_001393809.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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          "cds_length": 2280,
          "cdna_start": null,
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          "cdna_length": 5215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-231C>T",
          "hgvs_p": null,
          "transcript": "NM_001406881.1",
          "protein_id": "NP_001393810.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 759,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-664C>T",
          "hgvs_p": null,
          "transcript": "NM_001406882.1",
          "protein_id": "NP_001393811.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 759,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2280,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-205C>T",
          "hgvs_p": null,
          "transcript": "NM_001322007.2",
          "protein_id": "NP_001308936.1",
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          "aa_start": null,
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          "aa_length": 756,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4990,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-65C>T",
          "hgvs_p": null,
          "transcript": "NM_001322008.2",
          "protein_id": "NP_001308937.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": null,
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          "cdna_length": 4850,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-200C>T",
          "hgvs_p": null,
          "transcript": "NM_001406883.1",
          "protein_id": "NP_001393812.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": null,
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          "cdna_length": 4985,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
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          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-65C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699760.1",
          "protein_id": "ENSP00000514568.1",
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-580C>T",
          "hgvs_p": null,
          "transcript": "NM_001322009.2",
          "protein_id": "NP_001308938.1",
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          "aa_length": 738,
          "cds_start": -4,
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          "cdna_start": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.-390C>T",
          "hgvs_p": null,
          "transcript": "NM_001406887.1",
          "protein_id": "NP_001393816.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 738,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2217,
          "cdna_start": null,
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          "cdna_length": 5121,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
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      "computational_score_selected": 0.10399171710014343,
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      "computational_source_selected": "MetaRNN",
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      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "revel_prediction": "Uncertain_significance",
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      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.01,
      "bayesdelnoaf_prediction": "Uncertain_significance",
      "phylop100way_score": 0.74,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "acmg_classification": "Likely_benign",
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      "acmg_by_gene": [
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          "verdict": "Likely_benign",
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      "clinvar_disease": "Hereditary cancer-predisposing syndrome,Hereditary nonpolyposis colorectal neoplasms,Lynch syndrome 4",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "US:4",
      "phenotype_combined": "Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms|Lynch syndrome 4",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
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  "message": null
}