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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: 2-15167129-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=15167129&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 15167129,
      "ref": "A",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "NM_015909.4",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 52,
          "exon_rank_end": null,
          "exon_count": 52,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.7035T>G",
          "hgvs_p": "p.Ser2345Ser",
          "transcript": "NM_015909.4",
          "protein_id": "NP_056993.2",
          "transcript_support_level": null,
          "aa_start": 2345,
          "aa_end": null,
          "aa_length": 2371,
          "cds_start": 7035,
          "cds_end": null,
          "cds_length": 7116,
          "cdna_start": 7065,
          "cdna_end": null,
          "cdna_length": 7278,
          "mane_select": "ENST00000281513.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 52,
          "exon_rank_end": null,
          "exon_count": 52,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.7035T>G",
          "hgvs_p": "p.Ser2345Ser",
          "transcript": "ENST00000281513.10",
          "protein_id": "ENSP00000281513.5",
          "transcript_support_level": 1,
          "aa_start": 2345,
          "aa_end": null,
          "aa_length": 2371,
          "cds_start": 7035,
          "cds_end": null,
          "cds_length": 7116,
          "cdna_start": 7065,
          "cdna_end": null,
          "cdna_length": 7278,
          "mane_select": "NM_015909.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.4176T>G",
          "hgvs_p": "p.Ser1392Ser",
          "transcript": "ENST00000442506.5",
          "protein_id": "ENSP00000398411.1",
          "transcript_support_level": 1,
          "aa_start": 1392,
          "aa_end": null,
          "aa_length": 1418,
          "cds_start": 4176,
          "cds_end": null,
          "cds_length": 4257,
          "cdna_start": 4178,
          "cdna_end": null,
          "cdna_length": 4391,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.5019T>G",
          "hgvs_p": "p.Ser1673Ser",
          "transcript": "ENST00000700061.1",
          "protein_id": "ENSP00000514776.1",
          "transcript_support_level": null,
          "aa_start": 1673,
          "aa_end": null,
          "aa_length": 1699,
          "cds_start": 5019,
          "cds_end": null,
          "cds_length": 5100,
          "cdna_start": 5021,
          "cdna_end": null,
          "cdna_length": 5214,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.1545T>G",
          "hgvs_p": "p.Ser515Ser",
          "transcript": "ENST00000700063.1",
          "protein_id": "ENSP00000514778.1",
          "transcript_support_level": null,
          "aa_start": 515,
          "aa_end": null,
          "aa_length": 541,
          "cds_start": 1545,
          "cds_end": null,
          "cds_length": 1626,
          "cdna_start": 1546,
          "cdna_end": null,
          "cdna_length": 1714,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.474T>G",
          "hgvs_p": "p.Ser158Ser",
          "transcript": "ENST00000433283.5",
          "protein_id": "ENSP00000390920.1",
          "transcript_support_level": 2,
          "aa_start": 158,
          "aa_end": null,
          "aa_length": 184,
          "cds_start": 474,
          "cds_end": null,
          "cds_length": 555,
          "cdna_start": 474,
          "cdna_end": null,
          "cdna_length": 687,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 51,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.6906T>G",
          "hgvs_p": "p.Ser2302Ser",
          "transcript": "XM_011510357.3",
          "protein_id": "XP_011508659.1",
          "transcript_support_level": null,
          "aa_start": 2302,
          "aa_end": null,
          "aa_length": 2328,
          "cds_start": 6906,
          "cds_end": null,
          "cds_length": 6987,
          "cdna_start": 6936,
          "cdna_end": null,
          "cdna_length": 7149,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 51,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.6906T>G",
          "hgvs_p": "p.Ser2302Ser",
          "transcript": "XM_011510358.3",
          "protein_id": "XP_011508660.1",
          "transcript_support_level": null,
          "aa_start": 2302,
          "aa_end": null,
          "aa_length": 2328,
          "cds_start": 6906,
          "cds_end": null,
          "cds_length": 6987,
          "cdna_start": 6936,
          "cdna_end": null,
          "cdna_length": 7149,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 50,
          "exon_rank_end": null,
          "exon_count": 50,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.6777T>G",
          "hgvs_p": "p.Ser2259Ser",
          "transcript": "XM_047444734.1",
          "protein_id": "XP_047300690.1",
          "transcript_support_level": null,
          "aa_start": 2259,
          "aa_end": null,
          "aa_length": 2285,
          "cds_start": 6777,
          "cds_end": null,
          "cds_length": 6858,
          "cdna_start": 6807,
          "cdna_end": null,
          "cdna_length": 7020,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 46,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.6396T>G",
          "hgvs_p": "p.Ser2132Ser",
          "transcript": "XM_047444735.1",
          "protein_id": "XP_047300691.1",
          "transcript_support_level": null,
          "aa_start": 2132,
          "aa_end": null,
          "aa_length": 2158,
          "cds_start": 6396,
          "cds_end": null,
          "cds_length": 6477,
          "cdna_start": 6480,
          "cdna_end": null,
          "cdna_length": 6693,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.4836T>G",
          "hgvs_p": "p.Ser1612Ser",
          "transcript": "XM_011510360.3",
          "protein_id": "XP_011508662.1",
          "transcript_support_level": null,
          "aa_start": 1612,
          "aa_end": null,
          "aa_length": 1638,
          "cds_start": 4836,
          "cds_end": null,
          "cds_length": 4917,
          "cdna_start": 4900,
          "cdna_end": null,
          "cdna_length": 5113,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.4827T>G",
          "hgvs_p": "p.Ser1609Ser",
          "transcript": "XM_011510361.3",
          "protein_id": "XP_011508663.1",
          "transcript_support_level": null,
          "aa_start": 1609,
          "aa_end": null,
          "aa_length": 1635,
          "cds_start": 4827,
          "cds_end": null,
          "cds_length": 4908,
          "cdna_start": 4891,
          "cdna_end": null,
          "cdna_length": 5104,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.1586T>G",
          "hgvs_p": null,
          "transcript": "ENST00000485694.1",
          "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": 1798,
          "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": 35,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.*599T>G",
          "hgvs_p": null,
          "transcript": "ENST00000700062.1",
          "protein_id": "ENSP00000514777.1",
          "transcript_support_level": null,
          "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": 5203,
          "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": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.*335T>G",
          "hgvs_p": null,
          "transcript": "ENST00000700064.1",
          "protein_id": "ENSP00000514779.1",
          "transcript_support_level": null,
          "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": 3191,
          "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": 51,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.6869T>G",
          "hgvs_p": null,
          "transcript": "NR_052013.3",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 7082,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.*599T>G",
          "hgvs_p": null,
          "transcript": "ENST00000700062.1",
          "protein_id": "ENSP00000514777.1",
          "transcript_support_level": null,
          "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": 5203,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.*335T>G",
          "hgvs_p": null,
          "transcript": "ENST00000700064.1",
          "protein_id": "ENSP00000514779.1",
          "transcript_support_level": null,
          "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": 3191,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 53,
          "intron_rank": 51,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.6840+11859T>G",
          "hgvs_p": null,
          "transcript": "XM_017004317.2",
          "protein_id": "XP_016859806.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2293,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6882,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7118,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 53,
          "intron_rank": 51,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "c.6840+11859T>G",
          "hgvs_p": null,
          "transcript": "XM_047444733.1",
          "protein_id": "XP_047300689.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2293,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6882,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7367,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 54,
          "intron_rank": 51,
          "intron_rank_end": null,
          "gene_symbol": "NBAS",
          "gene_hgnc_id": 15625,
          "hgvs_c": "n.6870+11859T>G",
          "hgvs_p": null,
          "transcript": "XR_007076390.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 7254,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "NBAS",
      "gene_hgnc_id": 15625,
      "dbsnp": "rs1479190797",
      "frequency_reference_population": 0.000006569784,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.00000656978,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.028999999165534973,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "REVEL",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.029,
      "revel_prediction": "Benign",
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -1.01,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -3.104,
      "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": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_015909.4",
          "gene_symbol": "NBAS",
          "hgnc_id": 15625,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.7035T>G",
          "hgvs_p": "p.Ser2345Ser"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}