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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: 8-144511476-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=144511476&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 144511476,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000617875.6",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3582C>T",
          "hgvs_p": "p.Ala1194Ala",
          "transcript": "NM_004260.4",
          "protein_id": "NP_004251.4",
          "transcript_support_level": null,
          "aa_start": 1194,
          "aa_end": null,
          "aa_length": 1208,
          "cds_start": 3582,
          "cds_end": null,
          "cds_length": 3627,
          "cdna_start": 3631,
          "cdna_end": null,
          "cdna_length": 3819,
          "mane_select": "ENST00000617875.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3582C>T",
          "hgvs_p": "p.Ala1194Ala",
          "transcript": "ENST00000617875.6",
          "protein_id": "ENSP00000482313.2",
          "transcript_support_level": 1,
          "aa_start": 1194,
          "aa_end": null,
          "aa_length": 1208,
          "cds_start": 3582,
          "cds_end": null,
          "cds_length": 3627,
          "cdna_start": 3631,
          "cdna_end": null,
          "cdna_length": 3819,
          "mane_select": "NM_004260.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "ENST00000621189.4",
          "protein_id": "ENSP00000483145.1",
          "transcript_support_level": 1,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3708,
          "cdna_end": null,
          "cdna_length": 3896,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3657C>T",
          "hgvs_p": "p.Ala1219Ala",
          "transcript": "NM_001413019.1",
          "protein_id": "NP_001399948.1",
          "transcript_support_level": null,
          "aa_start": 1219,
          "aa_end": null,
          "aa_length": 1233,
          "cds_start": 3657,
          "cds_end": null,
          "cds_length": 3702,
          "cdna_start": 3706,
          "cdna_end": null,
          "cdna_length": 3894,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3591C>T",
          "hgvs_p": "p.Ala1197Ala",
          "transcript": "NM_001413036.1",
          "protein_id": "NP_001399965.1",
          "transcript_support_level": null,
          "aa_start": 1197,
          "aa_end": null,
          "aa_length": 1211,
          "cds_start": 3591,
          "cds_end": null,
          "cds_length": 3636,
          "cdna_start": 3640,
          "cdna_end": null,
          "cdna_length": 3828,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3552C>T",
          "hgvs_p": "p.Ala1184Ala",
          "transcript": "NM_001413039.1",
          "protein_id": "NP_001399968.1",
          "transcript_support_level": null,
          "aa_start": 1184,
          "aa_end": null,
          "aa_length": 1198,
          "cds_start": 3552,
          "cds_end": null,
          "cds_length": 3597,
          "cdna_start": 3601,
          "cdna_end": null,
          "cdna_length": 3789,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3486C>T",
          "hgvs_p": "p.Ala1162Ala",
          "transcript": "NM_001413020.1",
          "protein_id": "NP_001399949.1",
          "transcript_support_level": null,
          "aa_start": 1162,
          "aa_end": null,
          "aa_length": 1176,
          "cds_start": 3486,
          "cds_end": null,
          "cds_length": 3531,
          "cdna_start": 3535,
          "cdna_end": null,
          "cdna_length": 3723,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3453C>T",
          "hgvs_p": "p.Ala1151Ala",
          "transcript": "NM_001413025.1",
          "protein_id": "NP_001399954.1",
          "transcript_support_level": null,
          "aa_start": 1151,
          "aa_end": null,
          "aa_length": 1165,
          "cds_start": 3453,
          "cds_end": null,
          "cds_length": 3498,
          "cdna_start": 3502,
          "cdna_end": null,
          "cdna_length": 3690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3450C>T",
          "hgvs_p": "p.Ala1150Ala",
          "transcript": "NM_001413033.1",
          "protein_id": "NP_001399962.1",
          "transcript_support_level": null,
          "aa_start": 1150,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 3450,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3499,
          "cdna_end": null,
          "cdna_length": 3687,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3384C>T",
          "hgvs_p": "p.Ala1128Ala",
          "transcript": "NM_001413018.1",
          "protein_id": "NP_001399947.1",
          "transcript_support_level": null,
          "aa_start": 1128,
          "aa_end": null,
          "aa_length": 1142,
          "cds_start": 3384,
          "cds_end": null,
          "cds_length": 3429,
          "cdna_start": 3433,
          "cdna_end": null,
          "cdna_length": 3621,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3288C>T",
          "hgvs_p": "p.Ala1096Ala",
          "transcript": "NM_001413017.1",
          "protein_id": "NP_001399946.1",
          "transcript_support_level": null,
          "aa_start": 1096,
          "aa_end": null,
          "aa_length": 1110,
          "cds_start": 3288,
          "cds_end": null,
          "cds_length": 3333,
          "cdna_start": 3337,
          "cdna_end": null,
          "cdna_length": 3525,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.3231C>T",
          "hgvs_p": "p.Ala1077Ala",
          "transcript": "NM_001413029.1",
          "protein_id": "NP_001399958.1",
          "transcript_support_level": null,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1091,
          "cds_start": 3231,
          "cds_end": null,
          "cds_length": 3276,
          "cdna_start": 3280,
          "cdna_end": null,
          "cdna_length": 3468,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2586C>T",
          "hgvs_p": "p.Ala862Ala",
          "transcript": "NM_001413023.1",
          "protein_id": "NP_001399952.1",
          "transcript_support_level": null,
          "aa_start": 862,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": 2586,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": 3771,
          "cdna_end": null,
          "cdna_length": 3959,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2520C>T",
          "hgvs_p": "p.Ala840Ala",
          "transcript": "NM_001413041.1",
          "protein_id": "NP_001399970.1",
          "transcript_support_level": null,
          "aa_start": 840,
          "aa_end": null,
          "aa_length": 854,
          "cds_start": 2520,
          "cds_end": null,
          "cds_length": 2565,
          "cdna_start": 3767,
          "cdna_end": null,
          "cdna_length": 3955,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "NM_001413021.1",
          "protein_id": "NP_001399950.1",
          "transcript_support_level": null,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3345,
          "cdna_end": null,
          "cdna_length": 3533,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "NM_001413022.1",
          "protein_id": "NP_001399951.1",
          "transcript_support_level": null,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3696,
          "cdna_end": null,
          "cdna_length": 3884,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "NM_001413024.1",
          "protein_id": "NP_001399953.1",
          "transcript_support_level": null,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3593,
          "cdna_end": null,
          "cdna_length": 3781,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "NM_001413028.1",
          "protein_id": "NP_001399957.1",
          "transcript_support_level": null,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3421,
          "cdna_end": null,
          "cdna_length": 3609,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "NM_001413034.1",
          "protein_id": "NP_001399963.1",
          "transcript_support_level": null,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3600,
          "cdna_end": null,
          "cdna_length": 3788,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RECQL4",
          "gene_hgnc_id": 9949,
          "hgvs_c": "c.2511C>T",
          "hgvs_p": "p.Ala837Ala",
          "transcript": "NM_001413035.1",
          "protein_id": "NP_001399964.1",
          "transcript_support_level": null,
          "aa_start": 837,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 2511,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 3528,
          "cdna_end": null,
          "cdna_length": 3716,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
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      "splice_source_selected": "max_spliceai",
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      "phylop100way_score": 1.01,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "acmg_score": -11,
      "acmg_classification": "Benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Very_Strong,BP7",
      "acmg_by_gene": [
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          "pathogenic_score": 2,
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            "BP6_Very_Strong",
            "BP7"
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          "verdict": "Benign",
          "transcript": "ENST00000617875.6",
          "gene_symbol": "RECQL4",
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      ],
      "clinvar_disease": "Baller-Gerold syndrome,Inborn genetic diseases",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "Baller-Gerold syndrome|Inborn genetic diseases",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}