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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: 11-68025980-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=68025980&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 68025980,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_000694.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "NM_000694.4",
          "protein_id": "NP_000685.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000342456.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000694.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000342456.11",
          "protein_id": "ENSP00000473990.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_000694.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000342456.11"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000614849.4",
          "protein_id": "ENSP00000478486.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000614849.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1006-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000617288.4",
          "protein_id": "ENSP00000481604.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000617288.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1141-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894330.1",
          "protein_id": "ENSP00000564389.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000894330.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1123-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894328.1",
          "protein_id": "ENSP00000564387.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 470,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1413,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000894328.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "NM_001161473.3",
          "protein_id": "NP_001154945.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001161473.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894327.1",
          "protein_id": "ENSP00000564386.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000894327.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894329.1",
          "protein_id": "ENSP00000564388.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000894329.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894331.1",
          "protein_id": "ENSP00000564390.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000894331.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894332.1",
          "protein_id": "ENSP00000564391.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000894332.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
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          "transcript": "ENST00000894333.1",
          "protein_id": "ENSP00000564392.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
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          "cds_length": 1407,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
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          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894334.1",
          "protein_id": "ENSP00000564393.1",
          "transcript_support_level": null,
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          "cds_start": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000894335.1",
          "protein_id": "ENSP00000564394.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "gene_symbol": "ALDH3B1",
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          "hgvs_c": "c.1117-29A>G",
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1117-29A>G",
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          "transcript": "ENST00000894337.1",
          "protein_id": "ENSP00000564396.1",
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          "cds_start": null,
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          "feature": "ENST00000894337.1"
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        {
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          ],
          "exon_rank": null,
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          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.1006-29A>G",
          "hgvs_p": null,
          "transcript": "NM_001030010.3",
          "protein_id": "NP_001025181.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": null,
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          "cds_length": 1296,
          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "intron_rank": 7,
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          "gene_symbol": "ALDH3B1",
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          "hgvs_c": "c.1006-29A>G",
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          "transcript": "ENST00000894326.1",
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        },
        {
          "aa_ref": null,
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          ],
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          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
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          "hgvs_c": "c.766-29A>G",
          "hgvs_p": null,
          "transcript": "NM_001290058.2",
          "protein_id": "NP_001276987.1",
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          "aa_length": 351,
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          "biotype": "protein_coding",
          "feature": "NM_001290058.2"
        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3B1",
          "gene_hgnc_id": 410,
          "hgvs_c": "c.766-29A>G",
          "hgvs_p": null,
          "transcript": "ENST00000612297.4",
          "protein_id": "ENSP00000484901.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 351,
          "cds_start": null,
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          "cds_length": 1056,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000612297.4"
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
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          "biotype": "pseudogene",
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      ],
      "gene_symbol": "ALDH3B1",
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      "dbsnp": "rs2286164",
      "frequency_reference_population": 0.23107669,
      "hom_count_reference_population": 41766,
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      "gnomad_exomes_af": 0.227732,
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      "gnomad_genomes_homalt": 5658,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.949999988079071,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.95,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.845,
      "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": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_000694.4",
          "gene_symbol": "ALDH3B1",
          "hgnc_id": 410,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1117-29A>G",
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        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000532296.1",
          "gene_symbol": "GLTC1",
          "hgnc_id": 56861,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.341-648T>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
}