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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: 10-101019138-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=101019138&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 101019138,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000619208.6",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "NM_001195263.2",
          "protein_id": "NP_001182192.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 1033,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 3102,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 4112,
          "mane_select": "ENST00000619208.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "ENST00000619208.6",
          "protein_id": "ENSP00000480489.1",
          "transcript_support_level": 5,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 1033,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 3102,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 4112,
          "mane_select": "NM_001195263.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "NM_001437429.1",
          "protein_id": "NP_001424358.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 4109,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "ENST00000645349.1",
          "protein_id": "ENSP00000495283.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 573,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 1722,
          "cdna_start": 1205,
          "cdna_end": null,
          "cdna_length": 2126,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "ENST00000644782.1",
          "protein_id": "ENSP00000496747.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 2651,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "NM_001351044.2",
          "protein_id": "NP_001337973.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 539,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 1620,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 2012,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "NM_024895.5",
          "protein_id": "NP_079171.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 517,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 1554,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 1984,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "ENST00000370215.7",
          "protein_id": "ENSP00000359234.3",
          "transcript_support_level": 2,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 517,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 1554,
          "cdna_start": 1234,
          "cdna_end": null,
          "cdna_length": 2032,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_011540177.4",
          "protein_id": "XP_011538479.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 1033,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 3102,
          "cdna_start": 1403,
          "cdna_end": null,
          "cdna_length": 4285,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_047425767.1",
          "protein_id": "XP_047281723.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 1033,
          "cds_start": 1008,
          "cds_end": null,
          "cds_length": 3102,
          "cdna_start": 1791,
          "cdna_end": null,
          "cdna_length": 4673,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_047425768.1",
          "protein_id": "XP_047281724.1",
          "transcript_support_level": null,
          "aa_start": 336,
          "aa_end": null,
          "aa_length": 697,
          "cds_start": 1008,
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          "cds_length": 2094,
          "cdna_start": 1230,
          "cdna_end": null,
          "cdna_length": 2619,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
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          "exon_count": 15,
          "intron_rank": null,
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          "gene_symbol": "PDZD7",
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          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_011540179.4",
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          "cdna_start": 1230,
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        {
          "aa_ref": "P",
          "aa_alt": "P",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 8,
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          "exon_count": 10,
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          "gene_symbol": "PDZD7",
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          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_017016667.3",
          "protein_id": "XP_016872156.1",
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          "cds_start": 1008,
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        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
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          "intron_rank": null,
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          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_047425769.1",
          "protein_id": "XP_047281725.1",
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          "aa_end": null,
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        },
        {
          "aa_ref": "P",
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          "protein_coding": true,
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          ],
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          "hgvs_c": "c.1008C>T",
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        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 8,
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_011540181.4",
          "protein_id": "XP_011538483.1",
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        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro",
          "transcript": "XM_011540183.4",
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          "mane_select": null,
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        },
        {
          "aa_ref": "P",
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          ],
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          "intron_rank": null,
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          "gene_symbol": "PDZD7",
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          "hgvs_c": "c.1008C>T",
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        },
        {
          "aa_ref": "P",
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          "strand": false,
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            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "PDZD7",
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          "hgvs_c": "c.1008C>T",
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "n.*1186C>T",
          "hgvs_p": null,
          "transcript": "ENST00000474125.7",
          "protein_id": "ENSP00000474447.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 4306,
          "mane_select": null,
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          "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": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "n.1230C>T",
          "hgvs_p": null,
          "transcript": "XR_945816.4",
          "protein_id": null,
          "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": 1956,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PDZD7",
          "gene_hgnc_id": 26257,
          "hgvs_c": "n.*1186C>T",
          "hgvs_p": null,
          "transcript": "ENST00000474125.7",
          "protein_id": "ENSP00000474447.1",
          "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": 4306,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "PDZD7",
      "gene_hgnc_id": 26257,
      "dbsnp": "rs144469613",
      "frequency_reference_population": 0.0082284855,
      "hom_count_reference_population": 61,
      "allele_count_reference_population": 12719,
      "gnomad_exomes_af": 0.00836695,
      "gnomad_genomes_af": 0.00696249,
      "gnomad_exomes_ac": 11658,
      "gnomad_genomes_ac": 1061,
      "gnomad_exomes_homalt": 57,
      "gnomad_genomes_homalt": 4,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6700000166893005,
      "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": -0.67,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.235,
      "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": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -20,
          "benign_score": 20,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000619208.6",
          "gene_symbol": "PDZD7",
          "hgnc_id": 26257,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,Unknown",
          "hgvs_c": "c.1008C>T",
          "hgvs_p": "p.Pro336Pro"
        }
      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:3 B:5",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}