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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: 10-28175824-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=28175824&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 28175824,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_173496.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "NM_001318170.2",
          "protein_id": "NP_001305099.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000683449.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001318170.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000683449.1",
          "protein_id": "ENSP00000507917.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001318170.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000683449.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000375719.7",
          "protein_id": "ENSP00000364871.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000375719.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "n.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000496637.6",
          "protein_id": "ENSP00000473899.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000496637.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000893174.1",
          "protein_id": "ENSP00000563233.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893174.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "NM_173496.5",
          "protein_id": "NP_775767.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_173496.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000337532.9",
          "protein_id": "ENSP00000337907.5",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000337532.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000375732.5",
          "protein_id": "ENSP00000364884.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000375732.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000893162.1",
          "protein_id": "ENSP00000563221.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1731,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893162.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000893165.1",
          "protein_id": "ENSP00000563224.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 576,
          "cds_start": null,
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          "cds_length": 1731,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000893165.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000893168.1",
          "protein_id": "ENSP00000563227.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 576,
          "cds_start": null,
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          "cds_length": 1731,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893168.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 18,
          "intron_rank": 4,
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          "gene_symbol": "MPP7",
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          "hgvs_c": "c.157-25765C>T",
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          "cds_start": null,
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        {
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          "gene_symbol": "MPP7",
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          "hgvs_c": "c.157-25765C>T",
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          "transcript": "ENST00000935550.1",
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        {
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          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
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          "transcript": "ENST00000957212.1",
          "protein_id": "ENSP00000627271.1",
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        {
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          "gene_symbol": "MPP7",
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          "transcript": "ENST00000957214.1",
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        {
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          "transcript": "ENST00000893173.1",
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        {
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          "intron_rank": 4,
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          "gene_symbol": "MPP7",
          "gene_hgnc_id": 26542,
          "hgvs_c": "c.157-25765C>T",
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          "transcript": "ENST00000893163.1",
          "protein_id": "ENSP00000563222.1",
          "transcript_support_level": null,
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          "aa_length": 549,
          "cds_start": null,
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          "cdna_length": null,
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        },
        {
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          ],
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          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "XR_007061944.1"
        }
      ],
      "gene_symbol": "MPP7",
      "gene_hgnc_id": 26542,
      "dbsnp": "rs7068246",
      "frequency_reference_population": 0.29305258,
      "hom_count_reference_population": 7816,
      "allele_count_reference_population": 44510,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.293053,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 44510,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 7816,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9800000190734863,
      "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": -0.98,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.181,
      "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_173496.5",
          "gene_symbol": "MPP7",
          "hgnc_id": 26542,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.157-25765C>T",
          "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
}