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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: 4-83469032-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=83469032&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [
            "PM2",
            "PP3_Moderate"
          ],
          "effects": [
            "missense_variant",
            "splice_region_variant"
          ],
          "gene_symbol": "ABRAXAS1",
          "hgnc_id": 25829,
          "hgvs_c": "c.596G>A",
          "hgvs_p": "p.Ser199Asn",
          "inheritance_mode": "AR",
          "pathogenic_score": 4,
          "score": 4,
          "transcript": "NM_139076.3",
          "verdict": "Uncertain_significance"
        },
        {
          "benign_score": 0,
          "criteria": [
            "PM2",
            "PP3_Moderate"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "MRPS18C",
          "hgnc_id": 16633,
          "hgvs_c": "c.*37-307C>T",
          "hgvs_p": null,
          "inheritance_mode": "AR",
          "pathogenic_score": 4,
          "score": 4,
          "transcript": "ENST00000857155.1",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP3_Moderate",
      "acmg_score": 4,
      "allele_count_reference_population": 17,
      "alphamissense_prediction": null,
      "alphamissense_score": 0.1639,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.67,
      "chr": "4",
      "clinvar_classification": "Uncertain significance",
      "clinvar_disease": "not provided",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "US:2",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": 0.17420297861099243,
      "computational_source_selected": "MetaRNN",
      "consequences": [
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 409,
          "aa_ref": "S",
          "aa_start": 199,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4210,
          "cdna_start": 624,
          "cds_end": null,
          "cds_length": 1230,
          "cds_start": 596,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 9,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "NM_139076.3",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.596G>A",
          "hgvs_p": "p.Ser199Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000321945.12",
          "protein_coding": true,
          "protein_id": "NP_620775.2",
          "strand": false,
          "transcript": "NM_139076.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 409,
          "aa_ref": "S",
          "aa_start": 199,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4210,
          "cdna_start": 624,
          "cds_end": null,
          "cds_length": 1230,
          "cds_start": 596,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 9,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000321945.12",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.596G>A",
          "hgvs_p": "p.Ser199Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_139076.3",
          "protein_coding": true,
          "protein_id": "ENSP00000369857.3",
          "strand": false,
          "transcript": "ENST00000321945.12",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 198,
          "aa_ref": "S",
          "aa_start": 84,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 655,
          "cdna_start": 251,
          "cds_end": null,
          "cds_length": 597,
          "cds_start": 251,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 5,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000611288.4",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.251G>A",
          "hgvs_p": "p.Ser84Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000482434.1",
          "strand": false,
          "transcript": "ENST00000611288.4",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 405,
          "aa_ref": "S",
          "aa_start": 195,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1944,
          "cdna_start": 729,
          "cds_end": null,
          "cds_length": 1218,
          "cds_start": 584,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 9,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000856950.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.584G>A",
          "hgvs_p": "p.Ser195Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000527009.1",
          "strand": false,
          "transcript": "ENST00000856950.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 360,
          "aa_ref": "S",
          "aa_start": 150,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1869,
          "cdna_start": 775,
          "cds_end": null,
          "cds_length": 1083,
          "cds_start": 449,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 9,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000506553.5",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.449G>A",
          "hgvs_p": "p.Ser150Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000426763.1",
          "strand": false,
          "transcript": "ENST00000506553.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 349,
          "aa_ref": "S",
          "aa_start": 139,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2487,
          "cdna_start": 444,
          "cds_end": null,
          "cds_length": 1050,
          "cds_start": 416,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 8,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000917160.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.416G>A",
          "hgvs_p": "p.Ser139Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000587219.1",
          "strand": false,
          "transcript": "ENST00000917160.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 322,
          "aa_ref": "S",
          "aa_start": 112,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2575,
          "cdna_start": 411,
          "cds_end": null,
          "cds_length": 969,
          "cds_start": 335,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 7,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000856948.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.335G>A",
          "hgvs_p": "p.Ser112Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000527007.1",
          "strand": false,
          "transcript": "ENST00000856948.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 318,
          "aa_ref": "S",
          "aa_start": 108,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2386,
          "cdna_start": 351,
          "cds_end": null,
          "cds_length": 957,
          "cds_start": 323,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 7,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000917161.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.323G>A",
          "hgvs_p": "p.Ser108Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000587220.1",
          "strand": false,
          "transcript": "ENST00000917161.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 300,
          "aa_ref": "S",
          "aa_start": 90,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4143,
          "cdna_start": 557,
          "cds_end": null,
          "cds_length": 903,
          "cds_start": 269,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 8,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001345962.2",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.269G>A",
          "hgvs_p": "p.Ser90Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001332891.1",
          "strand": false,
          "transcript": "NM_001345962.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 219,
          "aa_ref": "S",
          "aa_start": 192,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 847,
          "cdna_start": 762,
          "cds_end": null,
          "cds_length": 660,
          "cds_start": 575,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000505489.5",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.575G>A",
          "hgvs_p": "p.Ser192Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000480277.1",
          "strand": false,
          "transcript": "ENST00000505489.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 369,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2521,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1110,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 8,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000856949.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.476+1171G>A",
          "hgvs_p": null,
          "intron_rank": 5,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000527008.1",
          "strand": false,
          "transcript": "ENST00000856949.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 282,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2279,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 849,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000949403.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "c.216-1494G>A",
          "hgvs_p": null,
          "intron_rank": 3,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000619462.1",
          "strand": false,
          "transcript": "ENST00000949403.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 142,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1572,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 429,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 7,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000857155.1",
          "gene_hgnc_id": 16633,
          "gene_symbol": "MRPS18C",
          "hgvs_c": "c.*37-307C>T",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000527214.1",
          "strand": true,
          "transcript": "ENST00000857155.1",
          "transcript_support_level": null
        },
        {
          "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": 2718,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 8,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000475656.6",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "n.*304G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000426080.1",
          "strand": false,
          "transcript": "ENST00000475656.6",
          "transcript_support_level": 2
        },
        {
          "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": 1898,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 4,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000504777.1",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "n.870G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000504777.1",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 933,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 9,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "XR_001741334.3",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "n.624G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "XR_001741334.3",
          "transcript_support_level": null
        },
        {
          "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": 2718,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 8,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000475656.6",
          "gene_hgnc_id": 25829,
          "gene_symbol": "ABRAXAS1",
          "hgvs_c": "n.*304G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000426080.1",
          "strand": false,
          "transcript": "ENST00000475656.6",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 442,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 2,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000509571.1",
          "gene_hgnc_id": 16633,
          "gene_symbol": "MRPS18C",
          "hgvs_c": "n.42-303C>T",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000509571.1",
          "transcript_support_level": 3
        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": "Pathogenic",
      "dbscsnv_ada_score": 0.999793773234196,
      "dbsnp": "rs1060503253",
      "effect": "missense_variant,splice_region_variant",
      "frequency_reference_population": 0.000010555518,
      "gene_hgnc_id": 25829,
      "gene_symbol": "ABRAXAS1",
      "gnomad_exomes_ac": 15,
      "gnomad_exomes_af": 0.0000102848,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_ac": 2,
      "gnomad_genomes_af": 0.0000131515,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_heteroplasmic": null,
      "gnomad_mito_homoplasmic": null,
      "hom_count_reference_population": 0,
      "mitotip_prediction": null,
      "mitotip_score": null,
      "pathogenicity_classification_combined": "Uncertain significance",
      "phenotype_combined": "not provided",
      "phylop100way_prediction": "Benign",
      "phylop100way_score": 3.172,
      "pos": 83469032,
      "ref": "C",
      "revel_prediction": "Benign",
      "revel_score": 0.106,
      "splice_prediction_selected": "Pathogenic",
      "splice_score_selected": 0.9259999990463257,
      "splice_source_selected": "dbscSNV1_RF",
      "spliceai_max_prediction": "Pathogenic",
      "spliceai_max_score": 0.71,
      "transcript": "NM_139076.3"
    }
  ]
}
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