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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: 8-143927875-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143927875&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 21,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "PLEC",
          "hgnc_id": 9069,
          "hgvs_c": "c.3789G>A",
          "hgvs_p": "p.Glu1263Glu",
          "inheritance_mode": "AR,AD",
          "pathogenic_score": 0,
          "score": -21,
          "transcript": "NM_201380.4",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_score": -21,
      "allele_count_reference_population": 24333,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.5,
      "chr": "8",
      "clinvar_classification": "Benign",
      "clinvar_disease": " Ogna type, with muscular dystrophy, with pyloric atresia,Autosomal recessive limb-girdle muscular dystrophy type 2Q,Epidermolysis bullosa simplex,Epidermolysis bullosa simplex 5B,Epidermolysis bullosa simplex 5C,Epidermolysis bullosa simplex with nail dystrophy,not provided,not specified",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:5",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.5,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "E",
          "aa_start": 1126,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14804,
          "cdna_start": 3514,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 3378,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "NM_201384.3",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3378G>A",
          "hgvs_p": "p.Glu1126Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000345136.8",
          "protein_coding": true,
          "protein_id": "NP_958786.1",
          "strand": false,
          "transcript": "NM_201384.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "E",
          "aa_start": 1126,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 14804,
          "cdna_start": 3514,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 3378,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000345136.8",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3378G>A",
          "hgvs_p": "p.Glu1126Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_201384.3",
          "protein_coding": true,
          "protein_id": "ENSP00000344848.3",
          "strand": false,
          "transcript": "ENST00000345136.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4533,
          "aa_ref": "E",
          "aa_start": 1112,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14683,
          "cdna_start": 3393,
          "cds_end": null,
          "cds_length": 13602,
          "cds_start": 3336,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "NM_201378.4",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3336G>A",
          "hgvs_p": "p.Glu1112Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": "ENST00000356346.7",
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958780.1",
          "strand": false,
          "transcript": "NM_201378.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4533,
          "aa_ref": "E",
          "aa_start": 1112,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14683,
          "cdna_start": 3393,
          "cds_end": null,
          "cds_length": 13602,
          "cds_start": 3336,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000356346.7",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3336G>A",
          "hgvs_p": "p.Glu1112Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": "NM_201378.4",
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000348702.3",
          "strand": false,
          "transcript": "ENST00000356346.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4684,
          "aa_ref": "E",
          "aa_start": 1263,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 15249,
          "cdna_start": 3959,
          "cds_end": null,
          "cds_length": 14055,
          "cds_start": 3789,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000322810.8",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3789G>A",
          "hgvs_p": "p.Glu1263Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000323856.4",
          "strand": false,
          "transcript": "ENST00000322810.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4574,
          "aa_ref": "E",
          "aa_start": 1153,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14787,
          "cdna_start": 3497,
          "cds_end": null,
          "cds_length": 13725,
          "cds_start": 3459,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 33,
          "exon_rank": 27,
          "exon_rank_end": null,
          "feature": "ENST00000436759.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3459G>A",
          "hgvs_p": "p.Glu1153Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000388180.2",
          "strand": false,
          "transcript": "ENST00000436759.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4551,
          "aa_ref": "E",
          "aa_start": 1130,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14689,
          "cdna_start": 3399,
          "cds_end": null,
          "cds_length": 13656,
          "cds_start": 3390,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000357649.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3390G>A",
          "hgvs_p": "p.Glu1130Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000350277.2",
          "strand": false,
          "transcript": "ENST00000357649.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "E",
          "aa_start": 1126,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14736,
          "cdna_start": 3446,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 3378,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000354589.7",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3378G>A",
          "hgvs_p": "p.Glu1126Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000346602.3",
          "strand": false,
          "transcript": "ENST00000354589.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4525,
          "aa_ref": "E",
          "aa_start": 1104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14751,
          "cdna_start": 3461,
          "cds_end": null,
          "cds_length": 13578,
          "cds_start": 3312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000354958.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3312G>A",
          "hgvs_p": "p.Glu1104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000347044.2",
          "strand": false,
          "transcript": "ENST00000354958.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4515,
          "aa_ref": "E",
          "aa_start": 1094,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14646,
          "cdna_start": 3356,
          "cds_end": null,
          "cds_length": 13548,
          "cds_start": 3282,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000398774.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3282G>A",
          "hgvs_p": "p.Glu1094Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000381756.2",
          "strand": false,
          "transcript": "ENST00000398774.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4684,
          "aa_ref": "E",
          "aa_start": 1263,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 15299,
          "cdna_start": 4009,
          "cds_end": null,
          "cds_length": 14055,
          "cds_start": 3789,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "NM_201380.4",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3789G>A",
          "hgvs_p": "p.Glu1263Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958782.1",
          "strand": false,
          "transcript": "NM_201380.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4591,
          "aa_ref": "E",
          "aa_start": 1170,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13782,
          "cdna_start": 3516,
          "cds_end": null,
          "cds_length": 13776,
          "cds_start": 3510,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 34,
          "exon_rank": 28,
          "exon_rank_end": null,
          "feature": "ENST00000528025.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3510G>A",
          "hgvs_p": "p.Glu1170Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000437303.2",
          "strand": false,
          "transcript": "ENST00000528025.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4574,
          "aa_ref": "E",
          "aa_start": 1153,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14798,
          "cdna_start": 3508,
          "cds_end": null,
          "cds_length": 13725,
          "cds_start": 3459,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 33,
          "exon_rank": 27,
          "exon_rank_end": null,
          "feature": "NM_000445.5",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3459G>A",
          "hgvs_p": "p.Glu1153Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_000436.2",
          "strand": false,
          "transcript": "NM_000445.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4570,
          "aa_ref": "E",
          "aa_start": 1149,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13713,
          "cdna_start": 3447,
          "cds_end": null,
          "cds_length": 13713,
          "cds_start": 3447,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000527096.5",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3447G>A",
          "hgvs_p": "p.Glu1149Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000434583.1",
          "strand": false,
          "transcript": "ENST00000527096.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4564,
          "aa_ref": "E",
          "aa_start": 1143,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13737,
          "cdna_start": 3471,
          "cds_end": null,
          "cds_length": 13695,
          "cds_start": 3429,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "ENST00000685198.1",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3429G>A",
          "hgvs_p": "p.Glu1143Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000510528.1",
          "strand": false,
          "transcript": "ENST00000685198.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4551,
          "aa_ref": "E",
          "aa_start": 1130,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14789,
          "cdna_start": 3499,
          "cds_end": null,
          "cds_length": 13656,
          "cds_start": 3390,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "NM_201383.3",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3390G>A",
          "hgvs_p": "p.Glu1130Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958785.1",
          "strand": false,
          "transcript": "NM_201383.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "E",
          "aa_start": 1126,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14763,
          "cdna_start": 3473,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 3378,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "NM_201382.4",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3378G>A",
          "hgvs_p": "p.Glu1126Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958784.1",
          "strand": false,
          "transcript": "NM_201382.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4525,
          "aa_ref": "E",
          "aa_start": 1104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14665,
          "cdna_start": 3375,
          "cds_end": null,
          "cds_length": 13578,
          "cds_start": 3312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 26,
          "exon_rank_end": null,
          "feature": "NM_201379.3",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.3312G>A",
          "hgvs_p": "p.Glu1104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958781.1",
          "strand": false,
          "transcript": "NM_201379.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 4524,
          "aa_ref": "E",
          "aa_start": 1103,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13588,
          "cdna_start": 3322,
          "cds_end": null,
          "cds_length": 13575,
          "cds_start": 3309,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
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        {
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          "protein_id": "XP_047277851.1",
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          "transcript": "XM_047421895.1",
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        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": null,
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      "dbsnp": "rs11991764",
      "effect": "synonymous_variant",
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      "gnomad_exomes_ac": 14018,
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      "pathogenicity_classification_combined": "Benign",
      "phenotype_combined": "not specified|Autosomal recessive limb-girdle muscular dystrophy type 2Q;Epidermolysis bullosa simplex 5B, with muscular dystrophy;Epidermolysis bullosa simplex, Ogna type;Epidermolysis bullosa simplex 5C, with pyloric atresia;Epidermolysis bullosa simplex with nail dystrophy|not provided",
      "phylop100way_prediction": "Benign",
      "phylop100way_score": 0.529,
      "pos": 143927875,
      "ref": "C",
      "revel_prediction": null,
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      "splice_prediction_selected": "Benign",
      "splice_score_selected": 0,
      "splice_source_selected": "max_spliceai",
      "spliceai_max_prediction": "Benign",
      "spliceai_max_score": 0,
      "transcript": "NM_201380.4"
    }
  ]
}
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