← Back to variant description

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: 21-44330285-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=44330285&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "21",
      "pos": 44330285,
      "ref": "A",
      "alt": "G",
      "effect": "synonymous_variant",
      "transcript": "ENST00000339818.9",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.684T>C",
          "hgvs_p": "p.Asp228Asp",
          "transcript": "NM_004928.3",
          "protein_id": "NP_004919.1",
          "transcript_support_level": null,
          "aa_start": 228,
          "aa_end": null,
          "aa_length": 256,
          "cds_start": 684,
          "cds_end": null,
          "cds_length": 771,
          "cdna_start": 880,
          "cdna_end": null,
          "cdna_length": 2221,
          "mane_select": "ENST00000339818.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.684T>C",
          "hgvs_p": "p.Asp228Asp",
          "transcript": "ENST00000339818.9",
          "protein_id": "ENSP00000344566.4",
          "transcript_support_level": 1,
          "aa_start": 228,
          "aa_end": null,
          "aa_length": 256,
          "cds_start": 684,
          "cds_end": null,
          "cds_length": 771,
          "cdna_start": 880,
          "cdna_end": null,
          "cdna_length": 2221,
          "mane_select": "NM_004928.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.1041T>C",
          "hgvs_p": "p.Asp347Asp",
          "transcript": "ENST00000397956.7",
          "protein_id": "ENSP00000381047.3",
          "transcript_support_level": 1,
          "aa_start": 347,
          "aa_end": null,
          "aa_length": 375,
          "cds_start": 1041,
          "cds_end": null,
          "cds_length": 1128,
          "cdna_start": 1240,
          "cdna_end": null,
          "cdna_length": 1634,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.681T>C",
          "hgvs_p": "p.Asp227Asp",
          "transcript": "ENST00000325223.7",
          "protein_id": "ENSP00000317302.7",
          "transcript_support_level": 1,
          "aa_start": 227,
          "aa_end": null,
          "aa_length": 255,
          "cds_start": 681,
          "cds_end": null,
          "cds_length": 768,
          "cdna_start": 889,
          "cdna_end": null,
          "cdna_length": 1283,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "n.797T>C",
          "hgvs_p": null,
          "transcript": "ENST00000496321.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1191,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.1041T>C",
          "hgvs_p": "p.Asp347Asp",
          "transcript": "NM_001271441.2",
          "protein_id": "NP_001258370.1",
          "transcript_support_level": null,
          "aa_start": 347,
          "aa_end": null,
          "aa_length": 375,
          "cds_start": 1041,
          "cds_end": null,
          "cds_length": 1128,
          "cdna_start": 1237,
          "cdna_end": null,
          "cdna_length": 2578,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.681T>C",
          "hgvs_p": "p.Asp227Asp",
          "transcript": "NM_001271440.2",
          "protein_id": "NP_001258369.1",
          "transcript_support_level": null,
          "aa_start": 227,
          "aa_end": null,
          "aa_length": 255,
          "cds_start": 681,
          "cds_end": null,
          "cds_length": 768,
          "cdna_start": 877,
          "cdna_end": null,
          "cdna_length": 2218,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.558T>C",
          "hgvs_p": "p.Asp186Asp",
          "transcript": "NM_001271442.1",
          "protein_id": "NP_001258371.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 214,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 645,
          "cdna_start": 797,
          "cdna_end": null,
          "cdna_length": 2138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.1119T>C",
          "hgvs_p": "p.Asp373Asp",
          "transcript": "XM_047440980.1",
          "protein_id": "XP_047296936.1",
          "transcript_support_level": null,
          "aa_start": 373,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 1119,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 1388,
          "cdna_end": null,
          "cdna_length": 2729,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.1116T>C",
          "hgvs_p": "p.Asp372Asp",
          "transcript": "XM_047440981.1",
          "protein_id": "XP_047296937.1",
          "transcript_support_level": null,
          "aa_start": 372,
          "aa_end": null,
          "aa_length": 400,
          "cds_start": 1116,
          "cds_end": null,
          "cds_length": 1203,
          "cdna_start": 1386,
          "cdna_end": null,
          "cdna_length": 2727,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.1044T>C",
          "hgvs_p": "p.Asp348Asp",
          "transcript": "XM_047440982.1",
          "protein_id": "XP_047296938.1",
          "transcript_support_level": null,
          "aa_start": 348,
          "aa_end": null,
          "aa_length": 376,
          "cds_start": 1044,
          "cds_end": null,
          "cds_length": 1131,
          "cdna_start": 1240,
          "cdna_end": null,
          "cdna_length": 2581,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.759T>C",
          "hgvs_p": "p.Asp253Asp",
          "transcript": "XM_006724051.4",
          "protein_id": "XP_006724114.1",
          "transcript_support_level": null,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 759,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": 1023,
          "cdna_end": null,
          "cdna_length": 2364,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.756T>C",
          "hgvs_p": "p.Asp252Asp",
          "transcript": "XM_047440983.1",
          "protein_id": "XP_047296939.1",
          "transcript_support_level": null,
          "aa_start": 252,
          "aa_end": null,
          "aa_length": 280,
          "cds_start": 756,
          "cds_end": null,
          "cds_length": 843,
          "cdna_start": 1020,
          "cdna_end": null,
          "cdna_length": 2361,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.720T>C",
          "hgvs_p": "p.Asp240Asp",
          "transcript": "XM_047440984.1",
          "protein_id": "XP_047296940.1",
          "transcript_support_level": null,
          "aa_start": 240,
          "aa_end": null,
          "aa_length": 268,
          "cds_start": 720,
          "cds_end": null,
          "cds_length": 807,
          "cdna_start": 3483,
          "cdna_end": null,
          "cdna_length": 4824,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.720T>C",
          "hgvs_p": "p.Asp240Asp",
          "transcript": "XM_047440985.1",
          "protein_id": "XP_047296941.1",
          "transcript_support_level": null,
          "aa_start": 240,
          "aa_end": null,
          "aa_length": 268,
          "cds_start": 720,
          "cds_end": null,
          "cds_length": 807,
          "cdna_start": 3473,
          "cdna_end": null,
          "cdna_length": 4814,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.720T>C",
          "hgvs_p": "p.Asp240Asp",
          "transcript": "XM_047440986.1",
          "protein_id": "XP_047296942.1",
          "transcript_support_level": null,
          "aa_start": 240,
          "aa_end": null,
          "aa_length": 268,
          "cds_start": 720,
          "cds_end": null,
          "cds_length": 807,
          "cdna_start": 1193,
          "cdna_end": null,
          "cdna_length": 2534,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "c.717T>C",
          "hgvs_p": "p.Asp239Asp",
          "transcript": "XM_047440987.1",
          "protein_id": "XP_047296943.1",
          "transcript_support_level": null,
          "aa_start": 239,
          "aa_end": null,
          "aa_length": 267,
          "cds_start": 717,
          "cds_end": null,
          "cds_length": 804,
          "cdna_start": 3481,
          "cdna_end": null,
          "cdna_length": 4822,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "n.4138T>C",
          "hgvs_p": null,
          "transcript": "ENST00000462742.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4532,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFAP410",
          "gene_hgnc_id": 1260,
          "hgvs_c": "n.260T>C",
          "hgvs_p": null,
          "transcript": "ENST00000470196.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 654,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000241728",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-239T>C",
          "hgvs_p": null,
          "transcript": "ENST00000422357.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 704,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000241728",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-64T>C",
          "hgvs_p": null,
          "transcript": "ENST00000444409.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 619,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CFAP410",
      "gene_hgnc_id": 1260,
      "dbsnp": "rs11552068",
      "frequency_reference_population": 0.00914608,
      "hom_count_reference_population": 711,
      "allele_count_reference_population": 14721,
      "gnomad_exomes_af": 0.00609367,
      "gnomad_genomes_af": 0.038354,
      "gnomad_exomes_ac": 8880,
      "gnomad_genomes_ac": 5841,
      "gnomad_exomes_homalt": 376,
      "gnomad_genomes_homalt": 335,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9300000071525574,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "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": -0.93,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.228,
      "phylop100way_prediction": "Benign",
      "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": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000339818.9",
          "gene_symbol": "CFAP410",
          "hgnc_id": 1260,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.684T>C",
          "hgvs_p": "p.Asp228Asp"
        },
        {
          "score": -20,
          "benign_score": 20,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000422357.5",
          "gene_symbol": "ENSG00000241728",
          "hgnc_id": null,
          "effects": [
            "upstream_gene_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.-239T>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:4",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}