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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: 6-42228523-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=42228523&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 42228523,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000695948.1",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3461C>G",
          "hgvs_p": "p.Pro1154Arg",
          "transcript": "NM_001395490.1",
          "protein_id": "NP_001382419.1",
          "transcript_support_level": null,
          "aa_start": 1154,
          "aa_end": null,
          "aa_length": 1212,
          "cds_start": 3461,
          "cds_end": null,
          "cds_length": 3639,
          "cdna_start": 4252,
          "cdna_end": null,
          "cdna_length": 7844,
          "mane_select": "ENST00000695948.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3461C>G",
          "hgvs_p": "p.Pro1154Arg",
          "transcript": "ENST00000695948.1",
          "protein_id": "ENSP00000512293.1",
          "transcript_support_level": null,
          "aa_start": 1154,
          "aa_end": null,
          "aa_length": 1212,
          "cds_start": 3461,
          "cds_end": null,
          "cds_length": 3639,
          "cdna_start": 4252,
          "cdna_end": null,
          "cdna_length": 7844,
          "mane_select": "NM_001395490.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3485C>G",
          "hgvs_p": "p.Pro1162Arg",
          "transcript": "ENST00000541110.5",
          "protein_id": "ENSP00000439689.1",
          "transcript_support_level": 1,
          "aa_start": 1162,
          "aa_end": null,
          "aa_length": 1220,
          "cds_start": 3485,
          "cds_end": null,
          "cds_length": 3663,
          "cdna_start": 4054,
          "cdna_end": null,
          "cdna_length": 7646,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3425C>G",
          "hgvs_p": "p.Pro1142Arg",
          "transcript": "ENST00000372922.8",
          "protein_id": "ENSP00000362013.4",
          "transcript_support_level": 1,
          "aa_start": 1142,
          "aa_end": null,
          "aa_length": 1200,
          "cds_start": 3425,
          "cds_end": null,
          "cds_length": 3603,
          "cdna_start": 3988,
          "cdna_end": null,
          "cdna_length": 7286,
          "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": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "n.*2659C>G",
          "hgvs_p": null,
          "transcript": "ENST00000372917.9",
          "protein_id": "ENSP00000362008.6",
          "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": 3919,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "n.*2659C>G",
          "hgvs_p": null,
          "transcript": "ENST00000372917.9",
          "protein_id": "ENSP00000362008.6",
          "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": 3919,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3485C>G",
          "hgvs_p": "p.Pro1162Arg",
          "transcript": "NM_001297573.2",
          "protein_id": "NP_001284502.1",
          "transcript_support_level": null,
          "aa_start": 1162,
          "aa_end": null,
          "aa_length": 1220,
          "cds_start": 3485,
          "cds_end": null,
          "cds_length": 3663,
          "cdna_start": 4227,
          "cdna_end": null,
          "cdna_length": 7819,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3425C>G",
          "hgvs_p": "p.Pro1142Arg",
          "transcript": "NM_001391983.1",
          "protein_id": "NP_001378912.1",
          "transcript_support_level": null,
          "aa_start": 1142,
          "aa_end": null,
          "aa_length": 1200,
          "cds_start": 3425,
          "cds_end": null,
          "cds_length": 3603,
          "cdna_start": 4008,
          "cdna_end": null,
          "cdna_length": 7600,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3425C>G",
          "hgvs_p": "p.Pro1142Arg",
          "transcript": "NM_033502.4",
          "protein_id": "NP_277037.1",
          "transcript_support_level": null,
          "aa_start": 1142,
          "aa_end": null,
          "aa_length": 1200,
          "cds_start": 3425,
          "cds_end": null,
          "cds_length": 3603,
          "cdna_start": 4167,
          "cdna_end": null,
          "cdna_length": 7759,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3425C>G",
          "hgvs_p": "p.Pro1142Arg",
          "transcript": "ENST00000695966.1",
          "protein_id": "ENSP00000512292.1",
          "transcript_support_level": null,
          "aa_start": 1142,
          "aa_end": null,
          "aa_length": 1200,
          "cds_start": 3425,
          "cds_end": null,
          "cds_length": 3603,
          "cdna_start": 4008,
          "cdna_end": null,
          "cdna_length": 7600,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
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          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3212C>G",
          "hgvs_p": "p.Pro1071Arg",
          "transcript": "NM_001391984.1",
          "protein_id": "NP_001378913.1",
          "transcript_support_level": null,
          "aa_start": 1071,
          "aa_end": null,
          "aa_length": 1129,
          "cds_start": 3212,
          "cds_end": null,
          "cds_length": 3390,
          "cdna_start": 3831,
          "cdna_end": null,
          "cdna_length": 7423,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3212C>G",
          "hgvs_p": "p.Pro1071Arg",
          "transcript": "ENST00000340840.6",
          "protein_id": "ENSP00000339438.2",
          "transcript_support_level": 5,
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          "aa_length": 1129,
          "cds_start": 3212,
          "cds_end": null,
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          "cdna_start": 3800,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3176C>G",
          "hgvs_p": "p.Pro1059Arg",
          "transcript": "ENST00000354325.2",
          "protein_id": "ENSP00000346285.2",
          "transcript_support_level": 5,
          "aa_start": 1059,
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          "aa_length": 1117,
          "cds_start": 3176,
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          "cds_length": 3354,
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        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3521C>G",
          "hgvs_p": "p.Pro1174Arg",
          "transcript": "XM_017011046.2",
          "protein_id": "XP_016866535.1",
          "transcript_support_level": null,
          "aa_start": 1174,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": 3521,
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          "cdna_start": 4312,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
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          ],
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          "intron_rank": null,
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          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3521C>G",
          "hgvs_p": "p.Pro1174Arg",
          "transcript": "XM_047419026.1",
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          "cdna_start": 4362,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3521C>G",
          "hgvs_p": "p.Pro1174Arg",
          "transcript": "XM_047419027.1",
          "protein_id": "XP_047274983.1",
          "transcript_support_level": null,
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          "aa_length": 1232,
          "cds_start": 3521,
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          "cdna_start": 4185,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3521C>G",
          "hgvs_p": "p.Pro1174Arg",
          "transcript": "XM_047419028.1",
          "protein_id": "XP_047274984.1",
          "transcript_support_level": null,
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          "cds_start": 3521,
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "TRERF1",
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          "hgvs_c": "c.3521C>G",
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          "transcript": "XM_047419029.1",
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        },
        {
          "aa_ref": "P",
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          ],
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          "gene_symbol": "TRERF1",
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          "hgvs_c": "c.3521C>G",
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          "transcript": "XM_047419030.1",
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        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.3521C>G",
          "hgvs_p": "p.Pro1174Arg",
          "transcript": "XM_047419031.1",
          "protein_id": "XP_047274987.1",
          "transcript_support_level": null,
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          "cds_start": 3521,
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          "cdna_start": 4228,
          "cdna_end": null,
          "cdna_length": 7820,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
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          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 626,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "TRERF1",
      "gene_hgnc_id": 18273,
      "dbsnp": "rs527323317",
      "frequency_reference_population": 6.840694e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84069e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.1542452573776245,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.062,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0973,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.47,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.366,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000695948.1",
          "gene_symbol": "TRERF1",
          "hgnc_id": 18273,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.3461C>G",
          "hgvs_p": "p.Pro1154Arg"
        },
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "XR_001744122.2",
          "gene_symbol": "LOC105375061",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.121+3664G>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}