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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: X-63674097-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=63674097&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 63674097,
      "ref": "G",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000671741.2",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.886C>A",
          "hgvs_p": "p.Arg296Arg",
          "transcript": "NM_001353921.2",
          "protein_id": "NP_001340850.1",
          "transcript_support_level": null,
          "aa_start": 296,
          "aa_end": null,
          "aa_length": 523,
          "cds_start": 886,
          "cds_end": null,
          "cds_length": 1572,
          "cdna_start": 955,
          "cdna_end": null,
          "cdna_length": 4702,
          "mane_select": "ENST00000671741.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.886C>A",
          "hgvs_p": "p.Arg296Arg",
          "transcript": "ENST00000671741.2",
          "protein_id": "ENSP00000500715.1",
          "transcript_support_level": null,
          "aa_start": 296,
          "aa_end": null,
          "aa_length": 523,
          "cds_start": 886,
          "cds_end": null,
          "cds_length": 1572,
          "cdna_start": 955,
          "cdna_end": null,
          "cdna_length": 4702,
          "mane_select": "NM_001353921.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "ENST00000253401.10",
          "protein_id": "ENSP00000253401.6",
          "transcript_support_level": 1,
          "aa_start": 289,
          "aa_end": null,
          "aa_length": 516,
          "cds_start": 865,
          "cds_end": null,
          "cds_length": 1551,
          "cdna_start": 1666,
          "cdna_end": null,
          "cdna_length": 5413,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.886C>A",
          "hgvs_p": "p.Arg296Arg",
          "transcript": "ENST00000374878.5",
          "protein_id": "ENSP00000364012.2",
          "transcript_support_level": 1,
          "aa_start": 296,
          "aa_end": null,
          "aa_length": 487,
          "cds_start": 886,
          "cds_end": null,
          "cds_length": 1464,
          "cdna_start": 1287,
          "cdna_end": null,
          "cdna_length": 2217,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.559C>A",
          "hgvs_p": "p.Arg187Arg",
          "transcript": "ENST00000624843.3",
          "protein_id": "ENSP00000485626.1",
          "transcript_support_level": 1,
          "aa_start": 187,
          "aa_end": null,
          "aa_length": 414,
          "cds_start": 559,
          "cds_end": null,
          "cds_length": 1245,
          "cdna_start": 1425,
          "cdna_end": null,
          "cdna_length": 2154,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "ENST00000374870.8",
          "protein_id": "ENSP00000364004.5",
          "transcript_support_level": 5,
          "aa_start": 289,
          "aa_end": null,
          "aa_length": 564,
          "cds_start": 865,
          "cds_end": null,
          "cds_length": 1695,
          "cdna_start": 1642,
          "cdna_end": null,
          "cdna_length": 4644,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.904C>A",
          "hgvs_p": "p.Arg302Arg",
          "transcript": "NM_001353923.1",
          "protein_id": "NP_001340852.1",
          "transcript_support_level": null,
          "aa_start": 302,
          "aa_end": null,
          "aa_length": 529,
          "cds_start": 904,
          "cds_end": null,
          "cds_length": 1590,
          "cdna_start": 915,
          "cdna_end": null,
          "cdna_length": 4662,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.904C>A",
          "hgvs_p": "p.Arg302Arg",
          "transcript": "ENST00000635729.1",
          "protein_id": "ENSP00000490940.1",
          "transcript_support_level": 5,
          "aa_start": 302,
          "aa_end": null,
          "aa_length": 529,
          "cds_start": 904,
          "cds_end": null,
          "cds_length": 1590,
          "cdna_start": 915,
          "cdna_end": null,
          "cdna_length": 1761,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "NM_001369030.1",
          "protein_id": "NP_001355959.1",
          "transcript_support_level": null,
          "aa_start": 289,
          "aa_end": null,
          "aa_length": 516,
          "cds_start": 865,
          "cds_end": null,
          "cds_length": 1551,
          "cdna_start": 1432,
          "cdna_end": null,
          "cdna_length": 5179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "NM_001369031.1",
          "protein_id": "NP_001355960.1",
          "transcript_support_level": null,
          "aa_start": 289,
          "aa_end": null,
          "aa_length": 516,
          "cds_start": 865,
          "cds_end": null,
          "cds_length": 1551,
          "cdna_start": 1428,
          "cdna_end": null,
          "cdna_length": 5175,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "NM_001369032.1",
          "protein_id": "NP_001355961.1",
          "transcript_support_level": null,
          "aa_start": 289,
          "aa_end": null,
          "aa_length": 516,
          "cds_start": 865,
          "cds_end": null,
          "cds_length": 1551,
          "cdna_start": 1672,
          "cdna_end": null,
          "cdna_length": 5419,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "NM_015185.3",
          "protein_id": "NP_056000.1",
          "transcript_support_level": null,
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          "cds_start": 865,
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          "cdna_start": 1676,
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          "mane_select": null,
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        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.865C>A",
          "hgvs_p": "p.Arg289Arg",
          "transcript": "ENST00000671907.1",
          "protein_id": "ENSP00000500829.1",
          "transcript_support_level": null,
          "aa_start": 289,
          "aa_end": null,
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          "cds_start": 865,
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          "cdna_start": 1387,
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          "biotype": null,
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        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.802C>A",
          "hgvs_p": "p.Arg268Arg",
          "transcript": "ENST00000638021.1",
          "protein_id": "ENSP00000490410.1",
          "transcript_support_level": 5,
          "aa_start": 268,
          "aa_end": null,
          "aa_length": 506,
          "cds_start": 802,
          "cds_end": null,
          "cds_length": 1521,
          "cdna_start": 1297,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
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          "strand": false,
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          ],
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          "gene_symbol": "ARHGEF9",
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          "hgvs_c": "c.802C>A",
          "hgvs_p": "p.Arg268Arg",
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.802C>A",
          "hgvs_p": "p.Arg268Arg",
          "transcript": "NM_001369033.1",
          "protein_id": "NP_001355962.1",
          "transcript_support_level": null,
          "aa_start": 268,
          "aa_end": null,
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          "cds_start": 802,
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          "cdna_start": 1665,
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          "feature": null
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        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 7,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.802C>A",
          "hgvs_p": "p.Arg268Arg",
          "transcript": "NM_001369034.1",
          "protein_id": "NP_001355963.1",
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          "cds_start": 802,
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          "cdna_start": 1421,
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          "cdna_length": 5168,
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        },
        {
          "aa_ref": "R",
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          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
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          "hgvs_p": "p.Arg268Arg",
          "transcript": "NM_001369035.1",
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        {
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          "strand": false,
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
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          "hgvs_c": "c.802C>A",
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        },
        {
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          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "ARHGEF9",
          "gene_hgnc_id": 14561,
          "hgvs_c": "c.802C>A",
          "hgvs_p": "p.Arg268Arg",
          "transcript": "NM_001369037.1",
          "protein_id": "NP_001355966.1",
          "transcript_support_level": null,
          "aa_start": 268,
          "aa_end": null,
          "aa_length": 495,
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          "cdna_start": 1628,
          "cdna_end": null,
          "cdna_length": 5375,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
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          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
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      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000671741.2",
          "gene_symbol": "ARHGEF9",
          "hgnc_id": 14561,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.886C>A",
          "hgvs_p": "p.Arg296Arg"
        }
      ],
      "clinvar_disease": " 8,Developmental and epileptic encephalopathy",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Developmental and epileptic encephalopathy, 8",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}