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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: 2-227699166-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=227699166&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 227699166,
      "ref": "A",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000644224.2",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.549T>G",
          "hgvs_p": "p.Ala183Ala",
          "transcript": "NM_025243.4",
          "protein_id": "NP_079519.1",
          "transcript_support_level": null,
          "aa_start": 183,
          "aa_end": null,
          "aa_length": 496,
          "cds_start": 549,
          "cds_end": null,
          "cds_length": 1491,
          "cdna_start": 637,
          "cdna_end": null,
          "cdna_length": 5213,
          "mane_select": "ENST00000644224.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.549T>G",
          "hgvs_p": "p.Ala183Ala",
          "transcript": "ENST00000644224.2",
          "protein_id": "ENSP00000495385.1",
          "transcript_support_level": null,
          "aa_start": 183,
          "aa_end": null,
          "aa_length": 496,
          "cds_start": 549,
          "cds_end": null,
          "cds_length": 1491,
          "cdna_start": 637,
          "cdna_end": null,
          "cdna_length": 5213,
          "mane_select": "NM_025243.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.549T>G",
          "hgvs_p": "p.Ala183Ala",
          "transcript": "ENST00000258403.8",
          "protein_id": "ENSP00000258403.3",
          "transcript_support_level": 1,
          "aa_start": 183,
          "aa_end": null,
          "aa_length": 496,
          "cds_start": 549,
          "cds_end": null,
          "cds_length": 1491,
          "cdna_start": 715,
          "cdna_end": null,
          "cdna_length": 3183,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.*574T>G",
          "hgvs_p": null,
          "transcript": "ENST00000425817.6",
          "protein_id": "ENSP00000397393.2",
          "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": 2761,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.*574T>G",
          "hgvs_p": null,
          "transcript": "ENST00000425817.6",
          "protein_id": "ENSP00000397393.2",
          "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": 2761,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.585T>G",
          "hgvs_p": "p.Ala195Ala",
          "transcript": "ENST00000646591.1",
          "protein_id": "ENSP00000496701.1",
          "transcript_support_level": null,
          "aa_start": 195,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": 585,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": 893,
          "cdna_end": null,
          "cdna_length": 2397,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.549T>G",
          "hgvs_p": "p.Ala183Ala",
          "transcript": "NM_001371411.1",
          "protein_id": "NP_001358340.1",
          "transcript_support_level": null,
          "aa_start": 183,
          "aa_end": null,
          "aa_length": 496,
          "cds_start": 549,
          "cds_end": null,
          "cds_length": 1491,
          "cdna_start": 727,
          "cdna_end": null,
          "cdna_length": 5303,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.549T>G",
          "hgvs_p": "p.Ala183Ala",
          "transcript": "NM_001371412.1",
          "protein_id": "NP_001358341.1",
          "transcript_support_level": null,
          "aa_start": 183,
          "aa_end": null,
          "aa_length": 496,
          "cds_start": 549,
          "cds_end": null,
          "cds_length": 1491,
          "cdna_start": 893,
          "cdna_end": null,
          "cdna_length": 5469,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.537T>G",
          "hgvs_p": "p.Ala179Ala",
          "transcript": "NM_001371413.1",
          "protein_id": "NP_001358342.1",
          "transcript_support_level": null,
          "aa_start": 179,
          "aa_end": null,
          "aa_length": 492,
          "cds_start": 537,
          "cds_end": null,
          "cds_length": 1479,
          "cdna_start": 833,
          "cdna_end": null,
          "cdna_length": 5409,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.537T>G",
          "hgvs_p": "p.Ala179Ala",
          "transcript": "NM_001371414.1",
          "protein_id": "NP_001358343.1",
          "transcript_support_level": null,
          "aa_start": 179,
          "aa_end": null,
          "aa_length": 492,
          "cds_start": 537,
          "cds_end": null,
          "cds_length": 1479,
          "cdna_start": 1212,
          "cdna_end": null,
          "cdna_length": 5788,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.585T>G",
          "hgvs_p": "p.Ala195Ala",
          "transcript": "XM_047445927.1",
          "protein_id": "XP_047301883.1",
          "transcript_support_level": null,
          "aa_start": 195,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": 585,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": 1066,
          "cdna_end": null,
          "cdna_length": 5642,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.*574T>G",
          "hgvs_p": null,
          "transcript": "ENST00000431622.6",
          "protein_id": "ENSP00000400627.1",
          "transcript_support_level": 4,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2593,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.739T>G",
          "hgvs_p": null,
          "transcript": "ENST00000642268.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1643,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.234T>G",
          "hgvs_p": null,
          "transcript": "ENST00000645923.1",
          "protein_id": "ENSP00000495010.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3209,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
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          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.279T>G",
          "hgvs_p": null,
          "transcript": "ENST00000676066.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 2938,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.*574T>G",
          "hgvs_p": null,
          "transcript": "ENST00000431622.6",
          "protein_id": "ENSP00000400627.1",
          "transcript_support_level": 4,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2593,
          "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": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.259+290T>G",
          "hgvs_p": null,
          "transcript": "ENST00000409287.5",
          "protein_id": "ENSP00000386298.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 92,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 279,
          "cdna_start": null,
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          "cdna_length": 644,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.151-320T>G",
          "hgvs_p": null,
          "transcript": "ENST00000645700.1",
          "protein_id": "ENSP00000495372.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 659,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "n.150+3003T>G",
          "hgvs_p": null,
          "transcript": "ENST00000647113.1",
          "protein_id": "ENSP00000494966.1",
          "transcript_support_level": null,
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2851,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC19A3",
          "gene_hgnc_id": 16266,
          "hgvs_c": "c.*38T>G",
          "hgvs_p": null,
          "transcript": "ENST00000456524.6",
          "protein_id": "ENSP00000399001.2",
          "transcript_support_level": 4,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 228,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 688,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 790,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "SLC19A3",
      "gene_hgnc_id": 16266,
      "dbsnp": "rs74693100",
      "frequency_reference_population": 6.8404694e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84047e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6299999952316284,
      "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": -0.63,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.863,
      "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_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000644224.2",
          "gene_symbol": "SLC19A3",
          "hgnc_id": 16266,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.549T>G",
          "hgvs_p": "p.Ala183Ala"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}