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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: 3-37813623-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=37813623&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 37813623,
      "ref": "C",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_002207.3",
      "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": 28,
          "intron_rank": 27,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.3010-5268C>T",
          "hgvs_p": null,
          "transcript": "NM_002207.3",
          "protein_id": "NP_002198.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000264741.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002207.3"
        },
        {
          "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": 28,
          "intron_rank": 27,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.3010-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000264741.10",
          "protein_id": "ENSP00000264741.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002207.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000264741.10"
        },
        {
          "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": 28,
          "intron_rank": 27,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.3007-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000921363.1",
          "protein_id": "ENSP00000591422.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1034,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3105,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000921363.1"
        },
        {
          "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": 28,
          "intron_rank": 27,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.3007-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000944256.1",
          "protein_id": "ENSP00000614315.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1034,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3105,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000944256.1"
        },
        {
          "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": 28,
          "intron_rank": 27,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.3001-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000944258.1",
          "protein_id": "ENSP00000614317.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000944258.1"
        },
        {
          "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": 27,
          "intron_rank": 26,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.2920-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000944260.1",
          "protein_id": "ENSP00000614319.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1005,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3018,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000944260.1"
        },
        {
          "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": 27,
          "intron_rank": 26,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.2884-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000944257.1",
          "protein_id": "ENSP00000614316.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 993,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2982,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000944257.1"
        },
        {
          "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": 27,
          "intron_rank": 26,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.2872-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000944261.1",
          "protein_id": "ENSP00000614320.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 989,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2970,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000944261.1"
        },
        {
          "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": 27,
          "intron_rank": 26,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.2869-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000944259.1",
          "protein_id": "ENSP00000614318.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 988,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2967,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000944259.1"
        },
        {
          "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": 26,
          "intron_rank": 25,
          "intron_rank_end": null,
          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.2788-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000921364.1",
          "protein_id": "ENSP00000591423.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 961,
          "cds_start": null,
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          "cds_length": 2886,
          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "exon_count": 3,
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          "gene_symbol": "ITGA9",
          "gene_hgnc_id": 6145,
          "hgvs_c": "c.109-5268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000411817.2",
          "protein_id": "ENSP00000406533.2",
          "transcript_support_level": 5,
          "aa_start": null,
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          "aa_length": 68,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        {
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          "gene_symbol": "ITGA9-AS1",
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          "hgvs_c": "n.251-4743G>A",
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        {
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          "gene_symbol": "ITGA9-AS1",
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        {
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          "hgvs_c": "n.325-4743G>A",
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          "transcript": "ENST00000430620.3",
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        {
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        {
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          "gene_symbol": "ITGA9-AS1",
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        {
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          "gene_symbol": "ITGA9-AS1",
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          "hgvs_c": "n.519-4743G>A",
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          "biotype": "pseudogene",
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        {
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        {
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        {
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          ],
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          "gene_symbol": "ITGA9-AS1",
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          "hgvs_c": "n.256+7391G>A",
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          "transcript": "NR_110531.1",
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          "mane_select": null,
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          "biotype": "pseudogene",
          "feature": "NR_110531.1"
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        {
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          "exon_count": 6,
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          "gene_symbol": "ITGA9-AS1",
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          "hgvs_c": "n.325+7391G>A",
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          "transcript": "NR_110532.1",
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "pseudogene",
          "feature": "NR_110532.1"
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      ],
      "gene_symbol": "ITGA9",
      "gene_hgnc_id": 6145,
      "dbsnp": "rs11129773",
      "frequency_reference_population": 0.04173072,
      "hom_count_reference_population": 170,
      "allele_count_reference_population": 6352,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.0417307,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 6352,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 170,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8700000047683716,
      "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": -0.87,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.643,
      "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_002207.3",
          "gene_symbol": "ITGA9",
          "hgnc_id": 6145,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.3010-5268C>T",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000630986.2",
          "gene_symbol": "ITGA9-AS1",
          "hgnc_id": 49668,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.204-4743G>A",
          "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
}