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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: 15-31028451-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=31028451&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "15",
      "pos": 31028451,
      "ref": "A",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "ENST00000256552.11",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3174T>A",
          "hgvs_p": "p.Asp1058Glu",
          "transcript": "NM_001252024.2",
          "protein_id": "NP_001238953.1",
          "transcript_support_level": null,
          "aa_start": 1058,
          "aa_end": null,
          "aa_length": 1625,
          "cds_start": 3174,
          "cds_end": null,
          "cds_length": 4878,
          "cdna_start": 3326,
          "cdna_end": null,
          "cdna_length": 5787,
          "mane_select": "ENST00000256552.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3174T>A",
          "hgvs_p": "p.Asp1058Glu",
          "transcript": "ENST00000256552.11",
          "protein_id": "ENSP00000256552.7",
          "transcript_support_level": 1,
          "aa_start": 1058,
          "aa_end": null,
          "aa_length": 1625,
          "cds_start": 3174,
          "cds_end": null,
          "cds_length": 4878,
          "cdna_start": 3326,
          "cdna_end": null,
          "cdna_length": 5787,
          "mane_select": "NM_001252024.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3225T>A",
          "hgvs_p": "p.Asp1075Glu",
          "transcript": "ENST00000558445.6",
          "protein_id": "ENSP00000452946.2",
          "transcript_support_level": 1,
          "aa_start": 1075,
          "aa_end": null,
          "aa_length": 1642,
          "cds_start": 3225,
          "cds_end": null,
          "cds_length": 4929,
          "cdna_start": 3426,
          "cdna_end": null,
          "cdna_length": 5887,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3108T>A",
          "hgvs_p": "p.Asp1036Glu",
          "transcript": "ENST00000397795.7",
          "protein_id": "ENSP00000380897.2",
          "transcript_support_level": 1,
          "aa_start": 1036,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 3108,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 3240,
          "cdna_end": null,
          "cdna_length": 5701,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.2877T>A",
          "hgvs_p": "p.Asp959Glu",
          "transcript": "ENST00000558768.5",
          "protein_id": "ENSP00000453119.2",
          "transcript_support_level": 1,
          "aa_start": 959,
          "aa_end": null,
          "aa_length": 1526,
          "cds_start": 2877,
          "cds_end": null,
          "cds_length": 4581,
          "cdna_start": 2877,
          "cdna_end": null,
          "cdna_length": 4581,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "n.*2060T>A",
          "hgvs_p": null,
          "transcript": "ENST00000560801.5",
          "protein_id": "ENSP00000453644.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4454,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "n.*2060T>A",
          "hgvs_p": null,
          "transcript": "ENST00000560801.5",
          "protein_id": "ENSP00000453644.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4454,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3225T>A",
          "hgvs_p": "p.Asp1075Glu",
          "transcript": "NM_001252020.2",
          "protein_id": "NP_001238949.1",
          "transcript_support_level": null,
          "aa_start": 1075,
          "aa_end": null,
          "aa_length": 1642,
          "cds_start": 3225,
          "cds_end": null,
          "cds_length": 4929,
          "cdna_start": 3426,
          "cdna_end": null,
          "cdna_length": 5887,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3126T>A",
          "hgvs_p": "p.Asp1042Glu",
          "transcript": "ENST00000711434.1",
          "protein_id": "ENSP00000518752.1",
          "transcript_support_level": null,
          "aa_start": 1042,
          "aa_end": null,
          "aa_length": 1609,
          "cds_start": 3126,
          "cds_end": null,
          "cds_length": 4830,
          "cdna_start": 3258,
          "cdna_end": null,
          "cdna_length": 5719,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.3108T>A",
          "hgvs_p": "p.Asp1036Glu",
          "transcript": "NM_002420.6",
          "protein_id": "NP_002411.3",
          "transcript_support_level": null,
          "aa_start": 1036,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 3108,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 3240,
          "cdna_end": null,
          "cdna_length": 5701,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "c.570T>A",
          "hgvs_p": "p.Asp190Glu",
          "transcript": "ENST00000559177.6",
          "protein_id": "ENSP00000453477.2",
          "transcript_support_level": 5,
          "aa_start": 190,
          "aa_end": null,
          "aa_length": 757,
          "cds_start": 570,
          "cds_end": null,
          "cds_length": 2274,
          "cdna_start": 570,
          "cdna_end": null,
          "cdna_length": 2274,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "n.549T>A",
          "hgvs_p": null,
          "transcript": "ENST00000557948.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 564,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1",
          "gene_hgnc_id": 7146,
          "hgvs_c": "n.397T>A",
          "hgvs_p": null,
          "transcript": "ENST00000558212.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 670,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000259720",
          "gene_hgnc_id": 58477,
          "hgvs_c": "n.260+1340A>T",
          "hgvs_p": null,
          "transcript": "ENST00000558755.1",
          "protein_id": null,
          "transcript_support_level": 4,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 565,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000259720",
          "gene_hgnc_id": 58477,
          "hgvs_c": "n.19-7302A>T",
          "hgvs_p": null,
          "transcript": "ENST00000561299.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 263,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000259720",
          "gene_hgnc_id": 58477,
          "hgvs_c": "n.218+1340A>T",
          "hgvs_p": null,
          "transcript": "ENST00000665655.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1841,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1-AS1",
          "gene_hgnc_id": 58477,
          "hgvs_c": "n.88+1340A>T",
          "hgvs_p": null,
          "transcript": "XR_007064555.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 953,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1-AS1",
          "gene_hgnc_id": 58477,
          "hgvs_c": "n.278+1340A>T",
          "hgvs_p": null,
          "transcript": "XR_932055.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 870,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "TRPM1-AS1",
          "gene_hgnc_id": 58477,
          "hgvs_c": "n.240+1340A>T",
          "hgvs_p": null,
          "transcript": "XR_932056.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1143,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "TRPM1",
      "gene_hgnc_id": 7146,
      "dbsnp": "rs748046539",
      "frequency_reference_population": 0.0000013681724,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 2,
      "gnomad_exomes_af": 0.00000136817,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.2665480971336365,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.21,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.8328,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.27,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.002,
      "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": 2,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP5,BP4",
      "acmg_by_gene": [
        {
          "score": 2,
          "benign_score": 1,
          "pathogenic_score": 3,
          "criteria": [
            "PM2",
            "PP5",
            "BP4"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000256552.11",
          "gene_symbol": "TRPM1",
          "hgnc_id": 7146,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.3174T>A",
          "hgvs_p": "p.Asp1058Glu"
        },
        {
          "score": 2,
          "benign_score": 1,
          "pathogenic_score": 3,
          "criteria": [
            "PM2",
            "PP5",
            "BP4"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000558755.1",
          "gene_symbol": "ENSG00000259720",
          "hgnc_id": 58477,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.260+1340A>T",
          "hgvs_p": null
        },
        {
          "score": 2,
          "benign_score": 1,
          "pathogenic_score": 3,
          "criteria": [
            "PM2",
            "PP5",
            "BP4"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "XR_932055.2",
          "gene_symbol": "TRPM1-AS1",
          "hgnc_id": 58477,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.278+1340A>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Congenital stationary night blindness",
      "clinvar_classification": "Likely pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Congenital stationary night blindness",
      "pathogenicity_classification_combined": "Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}