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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: 8-143817380-G-GC (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143817380&ref=G&alt=GC&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 143817380,
      "ref": "G",
      "alt": "GC",
      "effect": "frameshift_variant",
      "transcript": "NM_001362895.2",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1094dupG",
          "hgvs_p": "p.Thr366fs",
          "transcript": "NM_078480.3",
          "protein_id": "NP_510965.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1094,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000526683.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_078480.3"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1094dupG",
          "hgvs_p": "p.Thr366fs",
          "transcript": "ENST00000526683.6",
          "protein_id": "ENSP00000434359.1",
          "transcript_support_level": 1,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1094,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_078480.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000526683.6"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1043dupG",
          "hgvs_p": "p.Thr349fs",
          "transcript": "ENST00000349157.10",
          "protein_id": "ENSP00000322036.7",
          "transcript_support_level": 1,
          "aa_start": 348,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 1043,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000349157.10"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.965dupG",
          "hgvs_p": "p.Thr323fs",
          "transcript": "ENST00000453551.6",
          "protein_id": "ENSP00000402953.2",
          "transcript_support_level": 1,
          "aa_start": 322,
          "aa_end": null,
          "aa_length": 516,
          "cds_start": 965,
          "cds_end": null,
          "cds_length": 1551,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000453551.6"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.914dupG",
          "hgvs_p": "p.Thr306fs",
          "transcript": "ENST00000313352.11",
          "protein_id": "ENSP00000322016.7",
          "transcript_support_level": 1,
          "aa_start": 305,
          "aa_end": null,
          "aa_length": 499,
          "cds_start": 914,
          "cds_end": null,
          "cds_length": 1500,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000313352.11"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1205dupG",
          "hgvs_p": "p.Thr403fs",
          "transcript": "NM_001362895.2",
          "protein_id": "NP_001349824.1",
          "transcript_support_level": null,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1205,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001362895.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1205dupG",
          "hgvs_p": "p.Thr403fs",
          "transcript": "NM_001362896.2",
          "protein_id": "NP_001349825.1",
          "transcript_support_level": null,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1205,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001362896.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1205dupG",
          "hgvs_p": "p.Thr403fs",
          "transcript": "ENST00000533162.2",
          "protein_id": "ENSP00000433403.2",
          "transcript_support_level": 3,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1205,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000533162.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1205dupG",
          "hgvs_p": "p.Thr403fs",
          "transcript": "ENST00000703847.1",
          "protein_id": "ENSP00000515499.1",
          "transcript_support_level": null,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1205,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703847.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1169dupG",
          "hgvs_p": "p.Thr391fs",
          "transcript": "ENST00000533362.2",
          "protein_id": "ENSP00000515502.1",
          "transcript_support_level": 5,
          "aa_start": 390,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": 1169,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000533362.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1169dupG",
          "hgvs_p": "p.Thr391fs",
          "transcript": "ENST00000703850.1",
          "protein_id": "ENSP00000515503.1",
          "transcript_support_level": null,
          "aa_start": 390,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": 1169,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703850.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1154dupG",
          "hgvs_p": "p.Thr386fs",
          "transcript": "NM_001362897.2",
          "protein_id": "NP_001349826.1",
          "transcript_support_level": null,
          "aa_start": 385,
          "aa_end": null,
          "aa_length": 579,
          "cds_start": 1154,
          "cds_end": null,
          "cds_length": 1740,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001362897.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1094dupG",
          "hgvs_p": "p.Thr366fs",
          "transcript": "ENST00000703866.1",
          "protein_id": "ENSP00000515511.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1094,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000703866.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1091dupG",
          "hgvs_p": "p.Thr365fs",
          "transcript": "NM_001271098.2",
          "protein_id": "NP_001258027.1",
          "transcript_support_level": null,
          "aa_start": 364,
          "aa_end": null,
          "aa_length": 558,
          "cds_start": 1091,
          "cds_end": null,
          "cds_length": 1677,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001271098.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1091dupG",
          "hgvs_p": "p.Thr365fs",
          "transcript": "ENST00000527744.6",
          "protein_id": "ENSP00000436131.2",
          "transcript_support_level": 2,
          "aa_start": 364,
          "aa_end": null,
          "aa_length": 558,
          "cds_start": 1091,
          "cds_end": null,
          "cds_length": 1677,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000527744.6"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1088dupG",
          "hgvs_p": "p.Thr364fs",
          "transcript": "ENST00000963445.1",
          "protein_id": "ENSP00000633504.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 557,
          "cds_start": 1088,
          "cds_end": null,
          "cds_length": 1674,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000963445.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1067dupG",
          "hgvs_p": "p.Thr357fs",
          "transcript": "ENST00000897215.1",
          "protein_id": "ENSP00000567274.1",
          "transcript_support_level": null,
          "aa_start": 356,
          "aa_end": null,
          "aa_length": 550,
          "cds_start": 1067,
          "cds_end": null,
          "cds_length": 1653,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000897215.1"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1043dupG",
          "hgvs_p": "p.Thr349fs",
          "transcript": "NM_014281.5",
          "protein_id": "NP_055096.2",
          "transcript_support_level": null,
          "aa_start": 348,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 1043,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_014281.5"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1040dupG",
          "hgvs_p": "p.Thr348fs",
          "transcript": "NM_001271096.2",
          "protein_id": "NP_001258025.1",
          "transcript_support_level": null,
          "aa_start": 347,
          "aa_end": null,
          "aa_length": 541,
          "cds_start": 1040,
          "cds_end": null,
          "cds_length": 1626,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001271096.2"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1040dupG",
          "hgvs_p": "p.Thr348fs",
          "transcript": "ENST00000526459.6",
          "protein_id": "ENSP00000432610.2",
          "transcript_support_level": 2,
          "aa_start": 347,
          "aa_end": null,
          "aa_length": 541,
          "cds_start": 1040,
          "cds_end": null,
          "cds_length": 1626,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000532127.6"
        }
      ],
      "gene_symbol": "PUF60",
      "gene_hgnc_id": 17042,
      "dbsnp": "rs1085307139",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 4.593,
      "phylop100way_prediction": "Uncertain_significance",
      "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": 12,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 12,
          "benign_score": 0,
          "pathogenic_score": 12,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "NM_001362895.2",
          "gene_symbol": "PUF60",
          "hgnc_id": 17042,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1205dupG",
          "hgvs_p": "p.Thr403fs"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LP:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}
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