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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: 1-42556300-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=42556300&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "CCDC30",
          "hgnc_id": 26103,
          "hgvs_c": "c.1035G>A",
          "hgvs_p": "p.Met345Ile",
          "inheritance_mode": "AR",
          "pathogenic_score": 2,
          "score": 0,
          "transcript": "NM_001395517.1",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_score": 0,
      "allele_count_reference_population": 1,
      "alphamissense_prediction": null,
      "alphamissense_score": 0.1911,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.71,
      "chr": "1",
      "clinvar_classification": "Uncertain significance",
      "clinvar_disease": "not specified",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": 0.08591890335083008,
      "computational_source_selected": "MetaRNN",
      "consequences": [
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 938,
          "aa_ref": "M",
          "aa_start": 345,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6683,
          "cdna_start": 1739,
          "cds_end": null,
          "cds_length": 2817,
          "cds_start": 1035,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 21,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "NM_001395517.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.1035G>A",
          "hgvs_p": "p.Met345Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000657597.2",
          "protein_coding": true,
          "protein_id": "NP_001382446.1",
          "strand": true,
          "transcript": "NM_001395517.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 938,
          "aa_ref": "M",
          "aa_start": 345,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 6683,
          "cdna_start": 1739,
          "cds_end": null,
          "cds_length": 2817,
          "cds_start": 1035,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 21,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000657597.2",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.1035G>A",
          "hgvs_p": "p.Met345Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_001395517.1",
          "protein_coding": true,
          "protein_id": "ENSP00000499662.2",
          "strand": true,
          "transcript": "ENST00000657597.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 248,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6827,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 747,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 5,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000514642.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.28-9996G>A",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499505.1",
          "strand": true,
          "transcript": "ENST00000514642.1",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3653,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 23,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000477155.6",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "n.*975G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000421479.3",
          "strand": true,
          "transcript": "ENST00000477155.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3653,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 23,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000477155.6",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "n.*975G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000421479.3",
          "strand": true,
          "transcript": "ENST00000477155.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2445,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000507855.5",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "n.611-9996G>A",
          "hgvs_p": null,
          "intron_rank": 4,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000507855.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 826,
          "aa_ref": "M",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2689,
          "cdna_start": 828,
          "cds_end": null,
          "cds_length": 2481,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 18,
          "exon_rank": 7,
          "exon_rank_end": null,
          "feature": "ENST00000340612.6",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.699G>A",
          "hgvs_p": "p.Met233Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000340378.5",
          "strand": true,
          "transcript": "ENST00000340612.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 796,
          "aa_ref": "M",
          "aa_start": 264,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2553,
          "cdna_start": 793,
          "cds_end": null,
          "cds_length": 2391,
          "cds_start": 792,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 17,
          "exon_rank": 7,
          "exon_rank_end": null,
          "feature": "ENST00000671538.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.792G>A",
          "hgvs_p": "p.Met264Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499316.1",
          "strand": true,
          "transcript": "ENST00000671538.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 783,
          "aa_ref": "M",
          "aa_start": 190,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6318,
          "cdna_start": 1374,
          "cds_end": null,
          "cds_length": 2352,
          "cds_start": 570,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 17,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "NM_001080850.4",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.570G>A",
          "hgvs_p": "p.Met190Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001074319.1",
          "strand": true,
          "transcript": "NM_001080850.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 783,
          "aa_ref": "M",
          "aa_start": 190,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3098,
          "cdna_start": 680,
          "cds_end": null,
          "cds_length": 2352,
          "cds_start": 570,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 16,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000342022.8",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.570G>A",
          "hgvs_p": "p.Met190Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000339280.4",
          "strand": true,
          "transcript": "ENST00000342022.8",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 481,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6725,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1446,
          "cds_start": null,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_count": 23,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "NM_001355224.2",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.-475G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001342153.1",
          "strand": true,
          "transcript": "NM_001355224.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 752,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6125,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2259,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395379.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.583-9996G>A",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382308.1",
          "strand": true,
          "transcript": "NM_001395379.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5999,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395382.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382311.1",
          "strand": true,
          "transcript": "NM_001395382.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5758,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395383.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382312.1",
          "strand": true,
          "transcript": "NM_001395383.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6028,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395384.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382313.1",
          "strand": true,
          "transcript": "NM_001395384.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5991,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395385.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382314.1",
          "strand": true,
          "transcript": "NM_001395385.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3245,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000660083.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499483.1",
          "strand": true,
          "transcript": "ENST00000660083.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2929,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000664805.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499336.1",
          "strand": true,
          "transcript": "ENST00000664805.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2793,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000667205.1",
          "gene_hgnc_id": 26103,
          "gene_symbol": "CCDC30",
          "hgvs_c": "c.457-9996G>A",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499722.1",
          "strand": true,
          "transcript": "ENST00000667205.1",
          "transcript_support_level": null
        },
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}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.