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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: 8-140397625-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=140397625&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 140397625,
      "ref": "G",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "NM_001374682.1",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "NM_001160372.4",
          "protein_id": "NP_001153844.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000438773.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001160372.4"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000438773.4",
          "protein_id": "ENSP00000405060.3",
          "transcript_support_level": 1,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001160372.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000438773.4"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.658C>T",
          "hgvs_p": "p.Arg220*",
          "transcript": "ENST00000520857.5",
          "protein_id": "ENSP00000430116.1",
          "transcript_support_level": 1,
          "aa_start": 220,
          "aa_end": null,
          "aa_length": 991,
          "cds_start": 658,
          "cds_end": null,
          "cds_length": 2976,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000520857.5"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1150C>T",
          "hgvs_p": "p.Arg384*",
          "transcript": "NM_001374682.1",
          "protein_id": "NP_001361611.1",
          "transcript_support_level": null,
          "aa_start": 384,
          "aa_end": null,
          "aa_length": 1155,
          "cds_start": 1150,
          "cds_end": null,
          "cds_length": 3468,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001374682.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1150C>T",
          "hgvs_p": "p.Arg384*",
          "transcript": "ENST00000889106.1",
          "protein_id": "ENSP00000559165.1",
          "transcript_support_level": null,
          "aa_start": 384,
          "aa_end": null,
          "aa_length": 1155,
          "cds_start": 1150,
          "cds_end": null,
          "cds_length": 3468,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889106.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "NM_031466.8",
          "protein_id": "NP_113654.5",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_031466.8"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000648948.2",
          "protein_id": "ENSP00000498020.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000648948.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000889103.1",
          "protein_id": "ENSP00000559162.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889103.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000889105.1",
          "protein_id": "ENSP00000559164.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889105.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000889109.1",
          "protein_id": "ENSP00000559168.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889109.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000967712.1",
          "protein_id": "ENSP00000637771.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1146,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3441,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000967712.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1102C>T",
          "hgvs_p": "p.Arg368*",
          "transcript": "NM_001321646.2",
          "protein_id": "NP_001308575.1",
          "transcript_support_level": null,
          "aa_start": 368,
          "aa_end": null,
          "aa_length": 1139,
          "cds_start": 1102,
          "cds_end": null,
          "cds_length": 3420,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001321646.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1102C>T",
          "hgvs_p": "p.Arg368*",
          "transcript": "ENST00000920031.1",
          "protein_id": "ENSP00000590090.1",
          "transcript_support_level": null,
          "aa_start": 368,
          "aa_end": null,
          "aa_length": 1137,
          "cds_start": 1102,
          "cds_end": null,
          "cds_length": 3414,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000920031.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1102C>T",
          "hgvs_p": "p.Arg368*",
          "transcript": "ENST00000920035.1",
          "protein_id": "ENSP00000590094.1",
          "transcript_support_level": null,
          "aa_start": 368,
          "aa_end": null,
          "aa_length": 1136,
          "cds_start": 1102,
          "cds_end": null,
          "cds_length": 3411,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000920035.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "NM_001374683.1",
          "protein_id": "NP_001361612.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1111,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3336,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001374683.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000967713.1",
          "protein_id": "ENSP00000637772.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1111,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3336,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000967713.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1000C>T",
          "hgvs_p": "p.Arg334*",
          "transcript": "ENST00000889107.1",
          "protein_id": "ENSP00000559166.1",
          "transcript_support_level": null,
          "aa_start": 334,
          "aa_end": null,
          "aa_length": 1105,
          "cds_start": 1000,
          "cds_end": null,
          "cds_length": 3318,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889107.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1102C>T",
          "hgvs_p": "p.Arg368*",
          "transcript": "ENST00000920033.1",
          "protein_id": "ENSP00000590092.1",
          "transcript_support_level": null,
          "aa_start": 368,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1102,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000920033.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "NM_001374684.1",
          "protein_id": "NP_001361613.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1100,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3303,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001374684.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1129C>T",
          "hgvs_p": "p.Arg377*",
          "transcript": "ENST00000889102.1",
          "protein_id": "ENSP00000559161.1",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 1100,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 3303,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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      "computational_source_selected": "REVEL",
      "splice_score_selected": 0,
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      "splice_source_selected": "max_spliceai",
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      "bayesdelnoaf_score": 0.63,
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      "phylop100way_score": 6.799,
      "phylop100way_prediction": "Uncertain_significance",
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      "acmg_classification": "Pathogenic",
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      "clinvar_disease": " autosomal recessive 13,Abnormality of the nervous system,Intellectual disability,not provided",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:4",
      "phenotype_combined": "Intellectual disability, autosomal recessive 13|Abnormality of the nervous system|not provided",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
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  "message": null
}