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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: 3-51987188-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=51987188&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [
            "PS1_Moderate",
            "PM2"
          ],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "ABHD14A-ACY1",
          "hgnc_id": 38856,
          "hgvs_c": "c.969A>T",
          "hgvs_p": "p.Glu323Asp",
          "inheritance_mode": "",
          "pathogenic_score": 4,
          "score": 4,
          "transcript": "NM_001316331.2",
          "verdict": "Uncertain_significance"
        },
        {
          "benign_score": 0,
          "criteria": [
            "PS1_Moderate",
            "PM2"
          ],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "ACY1",
          "hgnc_id": 177,
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "inheritance_mode": "AR",
          "pathogenic_score": 4,
          "score": 4,
          "transcript": "NM_000666.3",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PS1_Moderate,PM2",
      "acmg_score": 4,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": 0.874,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Uncertain_significance",
      "bayesdelnoaf_score": 0.02,
      "chr": "3",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Uncertain_significance",
      "computational_score_selected": 0.6626187562942505,
      "computational_source_selected": "MetaRNN",
      "consequences": [
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1422,
          "cdna_start": 772,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "NM_000666.3",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000636358.2",
          "protein_coding": true,
          "protein_id": "NP_000657.1",
          "strand": true,
          "transcript": "NM_000666.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 1422,
          "cdna_start": 772,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000636358.2",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_000666.3",
          "protein_coding": true,
          "protein_id": "ENSP00000490149.1",
          "strand": true,
          "transcript": "ENST00000636358.2",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 509,
          "aa_ref": "E",
          "aa_start": 334,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 1705,
          "cdna_start": 1078,
          "cds_end": null,
          "cds_length": 1530,
          "cds_start": 1002,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 16,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000463937.1",
          "gene_hgnc_id": 38856,
          "gene_symbol": "ABHD14A-ACY1",
          "hgvs_c": "c.1002A>T",
          "hgvs_p": "p.Glu334Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000420487.1",
          "strand": true,
          "transcript": "ENST00000463937.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1473,
          "cdna_start": 825,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000404366.7",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000384296.2",
          "strand": true,
          "transcript": "ENST00000404366.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 584,
          "aa_ref": "E",
          "aa_start": 422,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1758,
          "cdna_start": 1268,
          "cds_end": null,
          "cds_length": 1756,
          "cds_start": 1266,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 17,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000637978.1",
          "gene_hgnc_id": 38856,
          "gene_symbol": "ABHD14A-ACY1",
          "hgvs_c": "c.1266A>T",
          "hgvs_p": "p.Glu422Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000490744.1",
          "strand": true,
          "transcript": "ENST00000637978.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 498,
          "aa_ref": "E",
          "aa_start": 323,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1836,
          "cdna_start": 1186,
          "cds_end": null,
          "cds_length": 1497,
          "cds_start": 969,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 17,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "NM_001316331.2",
          "gene_hgnc_id": 38856,
          "gene_symbol": "ABHD14A-ACY1",
          "hgvs_c": "c.969A>T",
          "hgvs_p": "p.Glu323Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001303260.1",
          "strand": true,
          "transcript": "NM_001316331.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1417,
          "cdna_start": 767,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "NM_001198895.2",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001185824.1",
          "strand": true,
          "transcript": "NM_001198895.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2365,
          "cdna_start": 1717,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 14,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000874798.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544857.1",
          "strand": true,
          "transcript": "ENST00000874798.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1430,
          "cdna_start": 782,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874801.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544860.1",
          "strand": true,
          "transcript": "ENST00000874801.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1410,
          "cdna_start": 758,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874809.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544868.1",
          "strand": true,
          "transcript": "ENST00000874809.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1389,
          "cdna_start": 741,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874811.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544870.1",
          "strand": true,
          "transcript": "ENST00000874811.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1459,
          "cdna_start": 811,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874812.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544871.1",
          "strand": true,
          "transcript": "ENST00000874812.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 408,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1408,
          "cdna_start": 780,
          "cds_end": null,
          "cds_length": 1227,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000953767.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000623826.1",
          "strand": true,
          "transcript": "ENST00000953767.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 407,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1504,
          "cdna_start": 853,
          "cds_end": null,
          "cds_length": 1224,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874802.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544861.1",
          "strand": true,
          "transcript": "ENST00000874802.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 407,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1416,
          "cdna_start": 765,
          "cds_end": null,
          "cds_length": 1224,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874807.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544866.1",
          "strand": true,
          "transcript": "ENST00000874807.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 407,
          "aa_ref": "E",
          "aa_start": 232,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1415,
          "cdna_start": 767,
          "cds_end": null,
          "cds_length": 1224,
          "cds_start": 696,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874813.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.696A>T",
          "hgvs_p": "p.Glu232Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544872.1",
          "strand": true,
          "transcript": "ENST00000874813.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 407,
          "aa_ref": "E",
          "aa_start": 233,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1383,
          "cdna_start": 758,
          "cds_end": null,
          "cds_length": 1224,
          "cds_start": 699,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874815.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.699A>T",
          "hgvs_p": "p.Glu233Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544874.1",
          "strand": true,
          "transcript": "ENST00000874815.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 406,
          "aa_ref": "E",
          "aa_start": 231,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1428,
          "cdna_start": 770,
          "cds_end": null,
          "cds_length": 1221,
          "cds_start": 693,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 15,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000874805.1",
          "gene_hgnc_id": 177,
          "gene_symbol": "ACY1",
          "hgvs_c": "c.693A>T",
          "hgvs_p": "p.Glu231Asp",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000544864.1",
          "strand": true,
          "transcript": "ENST00000874805.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "D",
          "aa_end": null,
          "aa_length": 403,
          "aa_ref": "E",
          "aa_start": 228,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1400,
          "cdna_start": 757,
          "cds_end": null,
          "cds_length": 1212,
          "cds_start": 684,
          "consequences": [
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  ]
}
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