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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: 1-150557296-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=150557296&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 150557296,
      "ref": "C",
      "alt": "T",
      "effect": "stop_gained",
      "transcript": "ENST00000271643.9",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "NM_019032.6",
          "protein_id": "NP_061905.2",
          "transcript_support_level": null,
          "aa_start": 670,
          "aa_end": null,
          "aa_length": 1074,
          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 3225,
          "cdna_start": 2258,
          "cdna_end": null,
          "cdna_length": 4212,
          "mane_select": "ENST00000271643.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "ENST00000271643.9",
          "protein_id": "ENSP00000271643.4",
          "transcript_support_level": 5,
          "aa_start": 670,
          "aa_end": null,
          "aa_length": 1074,
          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 3225,
          "cdna_start": 2258,
          "cdna_end": null,
          "cdna_length": 4212,
          "mane_select": "NM_019032.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "ENST00000369038.6",
          "protein_id": "ENSP00000358034.2",
          "transcript_support_level": 1,
          "aa_start": 670,
          "aa_end": null,
          "aa_length": 1074,
          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 3225,
          "cdna_start": 2209,
          "cdna_end": null,
          "cdna_length": 4167,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2077C>T",
          "hgvs_p": "p.Arg693*",
          "transcript": "NM_001288608.2",
          "protein_id": "NP_001275537.1",
          "transcript_support_level": null,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 1097,
          "cds_start": 2077,
          "cds_end": null,
          "cds_length": 3294,
          "cdna_start": 2327,
          "cdna_end": null,
          "cdna_length": 4285,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2077C>T",
          "hgvs_p": "p.Arg693*",
          "transcript": "ENST00000369039.9",
          "protein_id": "ENSP00000358035.5",
          "transcript_support_level": 5,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 1097,
          "cds_start": 2077,
          "cds_end": null,
          "cds_length": 3294,
          "cdna_start": 2366,
          "cdna_end": null,
          "cdna_length": 4319,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2077C>T",
          "hgvs_p": "p.Arg693*",
          "transcript": "ENST00000674043.1",
          "protein_id": "ENSP00000501295.1",
          "transcript_support_level": null,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 1097,
          "cds_start": 2077,
          "cds_end": null,
          "cds_length": 3294,
          "cdna_start": 2218,
          "cdna_end": null,
          "cdna_length": 3906,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "NM_001378596.1",
          "protein_id": "NP_001365525.1",
          "transcript_support_level": null,
          "aa_start": 670,
          "aa_end": null,
          "aa_length": 1074,
          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 3225,
          "cdna_start": 2636,
          "cdna_end": null,
          "cdna_length": 4590,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.1891C>T",
          "hgvs_p": "p.Arg631*",
          "transcript": "NM_001288607.2",
          "protein_id": "NP_001275536.1",
          "transcript_support_level": null,
          "aa_start": 631,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": 1891,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": 2141,
          "cdna_end": null,
          "cdna_length": 4095,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.1891C>T",
          "hgvs_p": "p.Arg631*",
          "transcript": "ENST00000674058.1",
          "protein_id": "ENSP00000501255.1",
          "transcript_support_level": null,
          "aa_start": 631,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": 1891,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": 2032,
          "cdna_end": null,
          "cdna_length": 3720,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "NM_025008.5",
          "protein_id": "NP_079284.2",
          "transcript_support_level": null,
          "aa_start": 670,
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          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 2634,
          "cdna_start": 2258,
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          "cdna_length": 2908,
          "mane_select": null,
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        },
        {
          "aa_ref": "R",
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          "strand": true,
          "consequences": [
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          ],
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          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "ENST00000369041.9",
          "protein_id": "ENSP00000358037.5",
          "transcript_support_level": 5,
          "aa_start": 670,
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          "aa_length": 877,
          "cds_start": 2008,
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          "cdna_start": 2258,
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          "mane_select": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 12,
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          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2176C>T",
          "hgvs_p": "p.Arg726*",
          "transcript": "XM_011509644.4",
          "protein_id": "XP_011507946.1",
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          "cds_start": 2176,
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        {
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          "consequences": [
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          ],
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          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2107C>T",
          "hgvs_p": "p.Arg703*",
          "transcript": "XM_047422819.1",
          "protein_id": "XP_047278775.1",
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        {
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          "strand": true,
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          "intron_rank": null,
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          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2077C>T",
          "hgvs_p": "p.Arg693*",
          "transcript": "XM_011509648.4",
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        {
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        {
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          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2077C>T",
          "hgvs_p": "p.Arg693*",
          "transcript": "XM_047422820.1",
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        {
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        {
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        {
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        },
        {
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          "intron_rank": null,
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          "gene_symbol": "ADAMTSL4",
          "gene_hgnc_id": 19706,
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*",
          "transcript": "XM_047422832.1",
          "protein_id": "XP_047278788.1",
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        {
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          "exon_count": 15,
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      ],
      "gene_symbol": "ADAMTSL4",
      "gene_hgnc_id": 19706,
      "dbsnp": "rs368482584",
      "frequency_reference_population": 0.000021092492,
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      "allele_count_reference_population": 34,
      "gnomad_exomes_af": 0.0000219209,
      "gnomad_genomes_af": 0.0000131446,
      "gnomad_exomes_ac": 32,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.5099999904632568,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.51,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 0.345,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "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": 16,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PP5_Very_Strong",
      "acmg_by_gene": [
        {
          "score": 16,
          "benign_score": 0,
          "pathogenic_score": 16,
          "criteria": [
            "PVS1",
            "PP5_Very_Strong"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000271643.9",
          "gene_symbol": "ADAMTSL4",
          "hgnc_id": 19706,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.2008C>T",
          "hgvs_p": "p.Arg670*"
        },
        {
          "score": 14,
          "benign_score": 0,
          "pathogenic_score": 14,
          "criteria": [
            "PM2",
            "PP3_Strong",
            "PP5_Very_Strong"
          ],
          "verdict": "Pathogenic",
          "transcript": "NR_187269.1",
          "gene_symbol": "ADAMTSL4-AS2",
          "hgnc_id": 40895,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.32+397G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": " autosomal recessive, isolated,Ectopia lentis 2,Ectopia lentis et pupillae,not provided",
      "clinvar_classification": "Pathogenic/Likely pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:4 LP:3",
      "phenotype_combined": "Ectopia lentis 2, isolated, autosomal recessive|not provided|Ectopia lentis et pupillae;Ectopia lentis 2, isolated, autosomal recessive|Ectopia lentis et pupillae",
      "pathogenicity_classification_combined": "Pathogenic/Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}