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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: 10-63215676-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=63215676&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 63215676,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000399262.7",
      "consequences": [
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.699C>T",
          "hgvs_p": "p.Val233Val",
          "transcript": "NM_032776.3",
          "protein_id": "NP_116165.1",
          "transcript_support_level": null,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 2540,
          "cds_start": 699,
          "cds_end": null,
          "cds_length": 7623,
          "cdna_start": 1014,
          "cdna_end": null,
          "cdna_length": 8758,
          "mane_select": "ENST00000399262.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.699C>T",
          "hgvs_p": "p.Val233Val",
          "transcript": "ENST00000399262.7",
          "protein_id": "ENSP00000382204.2",
          "transcript_support_level": 5,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 2540,
          "cds_start": 699,
          "cds_end": null,
          "cds_length": 7623,
          "cdna_start": 1014,
          "cdna_end": null,
          "cdna_length": 8758,
          "mane_select": "NM_032776.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "ENST00000542921.5",
          "protein_id": "ENSP00000444682.1",
          "transcript_support_level": 1,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 2358,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 7077,
          "cdna_start": 770,
          "cdna_end": null,
          "cdna_length": 8149,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "n.671C>T",
          "hgvs_p": null,
          "transcript": "ENST00000402544.5",
          "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": 8011,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.-170C>T",
          "hgvs_p": null,
          "transcript": "NM_001318153.2",
          "protein_id": "NP_001305082.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2252,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6759,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8695,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.585C>T",
          "hgvs_p": "p.Val195Val",
          "transcript": "NM_001322252.2",
          "protein_id": "NP_001309181.1",
          "transcript_support_level": null,
          "aa_start": 195,
          "aa_end": null,
          "aa_length": 2502,
          "cds_start": 585,
          "cds_end": null,
          "cds_length": 7509,
          "cdna_start": 900,
          "cdna_end": null,
          "cdna_length": 8644,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "NM_001282948.2",
          "protein_id": "NP_001269877.1",
          "transcript_support_level": null,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 2358,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 7077,
          "cdna_start": 947,
          "cdna_end": null,
          "cdna_length": 8691,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "NM_001318154.2",
          "protein_id": "NP_001305083.1",
          "transcript_support_level": null,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 2358,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 7077,
          "cdna_start": 684,
          "cdna_end": null,
          "cdna_length": 8428,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.42C>T",
          "hgvs_p": "p.Val14Val",
          "transcript": "NM_001322254.2",
          "protein_id": "NP_001309183.1",
          "transcript_support_level": null,
          "aa_start": 14,
          "aa_end": null,
          "aa_length": 2321,
          "cds_start": 42,
          "cds_end": null,
          "cds_length": 6966,
          "cdna_start": 841,
          "cdna_end": null,
          "cdna_length": 8585,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.42C>T",
          "hgvs_p": "p.Val14Val",
          "transcript": "NM_001322258.2",
          "protein_id": "NP_001309187.1",
          "transcript_support_level": null,
          "aa_start": 14,
          "aa_end": null,
          "aa_length": 2321,
          "cds_start": 42,
          "cds_end": null,
          "cds_length": 6966,
          "cdna_start": 578,
          "cdna_end": null,
          "cdna_length": 8322,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.537C>T",
          "hgvs_p": "p.Val179Val",
          "transcript": "XM_047424774.1",
          "protein_id": "XP_047280730.1",
          "transcript_support_level": null,
          "aa_start": 179,
          "aa_end": null,
          "aa_length": 2486,
          "cds_start": 537,
          "cds_end": null,
          "cds_length": 7461,
          "cdna_start": 4385,
          "cdna_end": null,
          "cdna_length": 12129,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "XM_017015897.2",
          "protein_id": "XP_016871386.1",
          "transcript_support_level": null,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 2358,
          "cds_start": 153,
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          "cds_length": 7077,
          "cdna_start": 570,
          "cdna_end": null,
          "cdna_length": 8314,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "XM_017015898.2",
          "protein_id": "XP_016871387.1",
          "transcript_support_level": null,
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          "aa_length": 2358,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 7077,
          "cdna_start": 13999,
          "cdna_end": null,
          "cdna_length": 21743,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "XM_047424772.1",
          "protein_id": "XP_047280728.1",
          "transcript_support_level": null,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 2358,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 7077,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 8494,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "XM_047424773.1",
          "protein_id": "XP_047280729.1",
          "transcript_support_level": null,
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          "cds_start": 153,
          "cds_end": null,
          "cds_length": 7077,
          "cdna_start": 636,
          "cdna_end": null,
          "cdna_length": 8380,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "XM_047424775.1",
          "protein_id": "XP_047280731.1",
          "transcript_support_level": null,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 1850,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 5553,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 6163,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.153C>T",
          "hgvs_p": "p.Val51Val",
          "transcript": "XM_011539508.3",
          "protein_id": "XP_011537810.1",
          "transcript_support_level": null,
          "aa_start": 51,
          "aa_end": null,
          "aa_length": 1518,
          "cds_start": 153,
          "cds_end": null,
          "cds_length": 4557,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 7323,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "n.579C>T",
          "hgvs_p": null,
          "transcript": "ENST00000469152.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 734,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "n.727C>T",
          "hgvs_p": null,
          "transcript": "NR_134512.2",
          "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": 8190,
          "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_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "c.-170C>T",
          "hgvs_p": null,
          "transcript": "NM_001318153.2",
          "protein_id": "NP_001305082.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2252,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6759,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8695,
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "JMJD1C",
          "gene_hgnc_id": 12313,
          "hgvs_c": "n.831-59C>T",
          "hgvs_p": null,
          "transcript": "ENST00000489372.4",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 913,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "JMJD1C",
      "gene_hgnc_id": 12313,
      "dbsnp": "rs74138760",
      "frequency_reference_population": 0.0009874395,
      "hom_count_reference_population": 8,
      "allele_count_reference_population": 1569,
      "gnomad_exomes_af": 0.000626424,
      "gnomad_genomes_af": 0.00439461,
      "gnomad_exomes_ac": 900,
      "gnomad_genomes_ac": 669,
      "gnomad_exomes_homalt": 5,
      "gnomad_genomes_homalt": 3,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.3199999928474426,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.03999999910593033,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.32,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 3.057,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.04,
      "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": -15,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -15,
          "benign_score": 15,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Very_Strong",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000399262.7",
          "gene_symbol": "JMJD1C",
          "hgnc_id": 12313,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.699C>T",
          "hgvs_p": "p.Val233Val"
        }
      ],
      "clinvar_disease": "Early myoclonic encephalopathy,JMJD1C-related disorder,not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "Early myoclonic encephalopathy|JMJD1C-related disorder|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}