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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: 11-68903959-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=68903959&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 68903959,
      "ref": "T",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "NM_002180.3",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala",
          "transcript": "NM_002180.3",
          "protein_id": "NP_002171.2",
          "transcript_support_level": null,
          "aa_start": 3,
          "aa_end": null,
          "aa_length": 993,
          "cds_start": 7,
          "cds_end": null,
          "cds_length": 2982,
          "cdna_start": 69,
          "cdna_end": null,
          "cdna_length": 3914,
          "mane_select": "ENST00000255078.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala",
          "transcript": "ENST00000255078.8",
          "protein_id": "ENSP00000255078.4",
          "transcript_support_level": 1,
          "aa_start": 3,
          "aa_end": null,
          "aa_length": 993,
          "cds_start": 7,
          "cds_end": null,
          "cds_length": 2982,
          "cdna_start": 69,
          "cdna_end": null,
          "cdna_length": 3914,
          "mane_select": "NM_002180.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala",
          "transcript": "ENST00000675615.1",
          "protein_id": "ENSP00000502413.1",
          "transcript_support_level": null,
          "aa_start": 3,
          "aa_end": null,
          "aa_length": 875,
          "cds_start": 7,
          "cds_end": null,
          "cds_length": 2628,
          "cdna_start": 97,
          "cdna_end": null,
          "cdna_length": 2914,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala",
          "transcript": "XM_047426881.1",
          "protein_id": "XP_047282837.1",
          "transcript_support_level": null,
          "aa_start": 3,
          "aa_end": null,
          "aa_length": 956,
          "cds_start": 7,
          "cds_end": null,
          "cds_length": 2871,
          "cdna_start": 69,
          "cdna_end": null,
          "cdna_length": 3015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala",
          "transcript": "XM_017017671.3",
          "protein_id": "XP_016873160.1",
          "transcript_support_level": null,
          "aa_start": 3,
          "aa_end": null,
          "aa_length": 546,
          "cds_start": 7,
          "cds_end": null,
          "cds_length": 1641,
          "cdna_start": 69,
          "cdna_end": null,
          "cdna_length": 1780,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala",
          "transcript": "XM_005273976.3",
          "protein_id": "XP_005274033.1",
          "transcript_support_level": null,
          "aa_start": 3,
          "aa_end": null,
          "aa_length": 540,
          "cds_start": 7,
          "cds_end": null,
          "cds_length": 1623,
          "cdna_start": 69,
          "cdna_end": null,
          "cdna_length": 2085,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "n.69T>G",
          "hgvs_p": null,
          "transcript": "ENST00000544541.1",
          "protein_id": null,
          "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,
          "cdna_end": null,
          "cdna_length": 479,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "n.7T>G",
          "hgvs_p": null,
          "transcript": "ENST00000545146.1",
          "protein_id": "ENSP00000456366.1",
          "transcript_support_level": 3,
          "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": 477,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "n.7T>G",
          "hgvs_p": null,
          "transcript": "ENST00000674955.1",
          "protein_id": "ENSP00000502463.1",
          "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": 2512,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "n.7T>G",
          "hgvs_p": null,
          "transcript": "ENST00000676173.2",
          "protein_id": "ENSP00000520445.1",
          "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": 4597,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "n.7T>G",
          "hgvs_p": null,
          "transcript": "ENST00000676228.1",
          "protein_id": "ENSP00000502375.1",
          "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": 2603,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "c.-149A>C",
          "hgvs_p": null,
          "transcript": "NM_181514.2",
          "protein_id": "NP_852615.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 205,
          "cds_start": -4,
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          "cds_length": 618,
          "cdna_start": null,
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          "cdna_length": 693,
          "mane_select": "ENST00000362034.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "c.-149A>C",
          "hgvs_p": null,
          "transcript": "ENST00000362034.7",
          "protein_id": "ENSP00000354580.2",
          "transcript_support_level": 1,
          "aa_start": null,
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          "aa_length": 205,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 693,
          "mane_select": "NM_181514.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "c.-417A>C",
          "hgvs_p": null,
          "transcript": "ENST00000567045.5",
          "protein_id": "ENSP00000457859.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": 195,
          "cds_start": -4,
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          "cds_length": 588,
          "cdna_start": null,
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          "cdna_length": 932,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "c.-417A>C",
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          "transcript": "NM_181515.2",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "c.-417A>C",
          "hgvs_p": null,
          "transcript": "ENST00000450904.6",
          "protein_id": "ENSP00000389400.2",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 120,
          "cds_start": -4,
          "cds_end": null,
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          "cdna_start": null,
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          "cdna_length": 662,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "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": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "n.-157A>C",
          "hgvs_p": null,
          "transcript": "ENST00000536637.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 557,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IGHMBP2",
          "gene_hgnc_id": 5542,
          "hgvs_c": "n.-33T>G",
          "hgvs_p": null,
          "transcript": "ENST00000539224.2",
          "protein_id": "ENSP00000440465.2",
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        },
        {
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          "canonical": false,
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          "consequences": [
            "upstream_gene_variant"
          ],
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          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "n.-149A>C",
          "hgvs_p": null,
          "transcript": "ENST00000541265.1",
          "protein_id": "ENSP00000445009.1",
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "n.-149A>C",
          "hgvs_p": null,
          "transcript": "ENST00000541279.1",
          "protein_id": "ENSP00000442243.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 764,
          "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": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MRPL21",
          "gene_hgnc_id": 14479,
          "hgvs_c": "n.-149A>C",
          "hgvs_p": null,
          "transcript": "ENST00000544567.5",
          "protein_id": "ENSP00000438837.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
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      ],
      "gene_symbol": "IGHMBP2",
      "gene_hgnc_id": 5542,
      "dbsnp": "rs751910797",
      "frequency_reference_population": 0.000010867425,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 17,
      "gnomad_exomes_af": 0.00000637339,
      "gnomad_genomes_af": 0.0000525673,
      "gnomad_exomes_ac": 9,
      "gnomad_genomes_ac": 8,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.10279569029808044,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.158,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0573,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.11,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.254,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_002180.3",
          "gene_symbol": "IGHMBP2",
          "hgnc_id": 5542,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.7T>G",
          "hgvs_p": "p.Ser3Ala"
        },
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_181514.2",
          "gene_symbol": "MRPL21",
          "hgnc_id": 14479,
          "effects": [
            "upstream_gene_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.-149A>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Autosomal recessive distal spinal muscular atrophy 1,Charcot-Marie-Tooth disease axonal type 2S",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "Charcot-Marie-Tooth disease axonal type 2S;Autosomal recessive distal spinal muscular atrophy 1",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}