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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: 8-144513073-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=144513073&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "8",
      "pos": 144513073,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000617875.6",
      "consequences": [
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2529G>A",
          "hgvs_p": "p.Lys843Lys",
          "transcript": "NM_004260.4",
          "protein_id": "NP_004251.4",
          "transcript_support_level": null,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1208,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3627,
          "cdna_start": 2578,
          "cdna_end": null,
          "cdna_length": 3819,
          "mane_select": "ENST00000617875.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2529G>A",
          "hgvs_p": "p.Lys843Lys",
          "transcript": "ENST00000617875.6",
          "protein_id": "ENSP00000482313.2",
          "transcript_support_level": 1,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1208,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3627,
          "cdna_start": 2578,
          "cdna_end": null,
          "cdna_length": 3819,
          "mane_select": "NM_004260.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "ENST00000621189.4",
          "protein_id": "ENSP00000483145.1",
          "transcript_support_level": 1,
          "aa_start": 486,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 1458,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 2655,
          "cdna_end": null,
          "cdna_length": 3896,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2529G>A",
          "hgvs_p": "p.Lys843Lys",
          "transcript": "NM_001413019.1",
          "protein_id": "NP_001399948.1",
          "transcript_support_level": null,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1233,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3702,
          "cdna_start": 2578,
          "cdna_end": null,
          "cdna_length": 3894,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2529G>A",
          "hgvs_p": "p.Lys843Lys",
          "transcript": "NM_001413036.1",
          "protein_id": "NP_001399965.1",
          "transcript_support_level": null,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1211,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3636,
          "cdna_start": 2578,
          "cdna_end": null,
          "cdna_length": 3828,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2499G>A",
          "hgvs_p": "p.Lys833Lys",
          "transcript": "NM_001413039.1",
          "protein_id": "NP_001399968.1",
          "transcript_support_level": null,
          "aa_start": 833,
          "aa_end": null,
          "aa_length": 1198,
          "cds_start": 2499,
          "cds_end": null,
          "cds_length": 3597,
          "cdna_start": 2548,
          "cdna_end": null,
          "cdna_length": 3789,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2433G>A",
          "hgvs_p": "p.Lys811Lys",
          "transcript": "NM_001413020.1",
          "protein_id": "NP_001399949.1",
          "transcript_support_level": null,
          "aa_start": 811,
          "aa_end": null,
          "aa_length": 1176,
          "cds_start": 2433,
          "cds_end": null,
          "cds_length": 3531,
          "cdna_start": 2482,
          "cdna_end": null,
          "cdna_length": 3723,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2400G>A",
          "hgvs_p": "p.Lys800Lys",
          "transcript": "NM_001413025.1",
          "protein_id": "NP_001399954.1",
          "transcript_support_level": null,
          "aa_start": 800,
          "aa_end": null,
          "aa_length": 1165,
          "cds_start": 2400,
          "cds_end": null,
          "cds_length": 3498,
          "cdna_start": 2449,
          "cdna_end": null,
          "cdna_length": 3690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2397G>A",
          "hgvs_p": "p.Lys799Lys",
          "transcript": "NM_001413033.1",
          "protein_id": "NP_001399962.1",
          "transcript_support_level": null,
          "aa_start": 799,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2397,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 2446,
          "cdna_end": null,
          "cdna_length": 3687,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2331G>A",
          "hgvs_p": "p.Lys777Lys",
          "transcript": "NM_001413018.1",
          "protein_id": "NP_001399947.1",
          "transcript_support_level": null,
          "aa_start": 777,
          "aa_end": null,
          "aa_length": 1142,
          "cds_start": 2331,
          "cds_end": null,
          "cds_length": 3429,
          "cdna_start": 2380,
          "cdna_end": null,
          "cdna_length": 3621,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2235G>A",
          "hgvs_p": "p.Lys745Lys",
          "transcript": "NM_001413017.1",
          "protein_id": "NP_001399946.1",
          "transcript_support_level": null,
          "aa_start": 745,
          "aa_end": null,
          "aa_length": 1110,
          "cds_start": 2235,
          "cds_end": null,
          "cds_length": 3333,
          "cdna_start": 2284,
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          "cdna_length": 3525,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2178G>A",
          "hgvs_p": "p.Lys726Lys",
          "transcript": "NM_001413029.1",
          "protein_id": "NP_001399958.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 1091,
          "cds_start": 2178,
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          "cds_length": 3276,
          "cdna_start": 2227,
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          "cdna_length": 3468,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413023.1",
          "protein_id": "NP_001399952.1",
          "transcript_support_level": null,
          "aa_start": 486,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": 1458,
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          "cds_length": 2631,
          "cdna_start": 2643,
          "cdna_end": null,
          "cdna_length": 3959,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1392G>A",
          "hgvs_p": "p.Lys464Lys",
          "transcript": "NM_001413041.1",
          "protein_id": "NP_001399970.1",
          "transcript_support_level": null,
          "aa_start": 464,
          "aa_end": null,
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          "cds_start": 1392,
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          "cds_length": 2565,
          "cdna_start": 2639,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
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          "exon_count": 20,
          "intron_rank": null,
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          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413021.1",
          "protein_id": "NP_001399950.1",
          "transcript_support_level": null,
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          "cds_start": 1458,
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          "cdna_start": 2292,
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          "cdna_length": 3533,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413022.1",
          "protein_id": "NP_001399951.1",
          "transcript_support_level": null,
          "aa_start": 486,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 1458,
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          "cdna_start": 2643,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
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          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413024.1",
          "protein_id": "NP_001399953.1",
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        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_rank_end": null,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413028.1",
          "protein_id": "NP_001399957.1",
          "transcript_support_level": null,
          "aa_start": 486,
          "aa_end": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 15,
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          "exon_count": 21,
          "intron_rank": null,
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          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413034.1",
          "protein_id": "NP_001399963.1",
          "transcript_support_level": null,
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          "cdna_start": 2547,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.1458G>A",
          "hgvs_p": "p.Lys486Lys",
          "transcript": "NM_001413035.1",
          "protein_id": "NP_001399964.1",
          "transcript_support_level": null,
          "aa_start": 486,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 1458,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 2475,
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          "cdna_length": 3716,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
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            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000617875.6",
          "gene_symbol": "RECQL4",
          "hgnc_id": 9949,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.2529G>A",
          "hgvs_p": "p.Lys843Lys"
        },
        {
          "score": -4,
          "benign_score": 6,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000580385.1",
          "gene_symbol": "ENSG00000265393",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.271+236C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Baller-Gerold syndrome",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Baller-Gerold syndrome",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}