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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: 20-50893503-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=50893503&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 50893503,
      "ref": "G",
      "alt": "T",
      "effect": "stop_gained",
      "transcript": "ENST00000621696.5",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "NM_001282531.3",
          "protein_id": "NP_001269460.1",
          "transcript_support_level": null,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 2087,
          "cdna_end": null,
          "cdna_length": 6672,
          "mane_select": "ENST00000621696.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "ENST00000621696.5",
          "protein_id": "ENSP00000483881.1",
          "transcript_support_level": 5,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 2087,
          "cdna_end": null,
          "cdna_length": 6672,
          "mane_select": "NM_001282531.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "ENST00000349014.8",
          "protein_id": "ENSP00000342905.3",
          "transcript_support_level": 1,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 1508,
          "cdna_end": null,
          "cdna_length": 4662,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "ENST00000371602.9",
          "protein_id": "ENSP00000360662.2",
          "transcript_support_level": 1,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 2773,
          "cdna_end": null,
          "cdna_length": 7360,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "ENST00000396029.8",
          "protein_id": "ENSP00000379346.3",
          "transcript_support_level": 1,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 1941,
          "cdna_end": null,
          "cdna_length": 6396,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1427C>A",
          "hgvs_p": "p.Ser476*",
          "transcript": "NM_001439000.1",
          "protein_id": "NP_001425929.1",
          "transcript_support_level": null,
          "aa_start": 476,
          "aa_end": null,
          "aa_length": 1174,
          "cds_start": 1427,
          "cds_end": null,
          "cds_length": 3525,
          "cdna_start": 2046,
          "cdna_end": null,
          "cdna_length": 6631,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1427C>A",
          "hgvs_p": "p.Ser476*",
          "transcript": "ENST00000673732.1",
          "protein_id": "ENSP00000501294.1",
          "transcript_support_level": null,
          "aa_start": 476,
          "aa_end": null,
          "aa_length": 1174,
          "cds_start": 1427,
          "cds_end": null,
          "cds_length": 3525,
          "cdna_start": 2046,
          "cdna_end": null,
          "cdna_length": 6631,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "NM_001282532.2",
          "protein_id": "NP_001269461.1",
          "transcript_support_level": null,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 1508,
          "cdna_end": null,
          "cdna_length": 6093,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "NM_001347511.2",
          "protein_id": "NP_001334440.1",
          "transcript_support_level": null,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 1912,
          "cdna_end": null,
          "cdna_length": 6497,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "NM_015339.5",
          "protein_id": "NP_056154.1",
          "transcript_support_level": null,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 2003,
          "cdna_end": null,
          "cdna_length": 6588,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "NM_181442.4",
          "protein_id": "NP_852107.1",
          "transcript_support_level": null,
          "aa_start": 404,
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          "aa_length": 1102,
          "cds_start": 1211,
          "cds_end": null,
          "cds_length": 3309,
          "cdna_start": 1828,
          "cdna_end": null,
          "cdna_length": 6413,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "ENST00000396032.8",
          "protein_id": "ENSP00000379349.2",
          "transcript_support_level": 2,
          "aa_start": 404,
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          "cds_start": 1211,
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          "cdna_start": 1812,
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          "cdna_length": 4979,
          "mane_select": null,
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 3,
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          "exon_count": 3,
          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.527C>A",
          "hgvs_p": "p.Ser176*",
          "transcript": "NM_001439001.1",
          "protein_id": "NP_001425930.1",
          "transcript_support_level": null,
          "aa_start": 176,
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          "cds_start": 527,
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          "cds_length": 2625,
          "cdna_start": 1715,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.527C>A",
          "hgvs_p": "p.Ser176*",
          "transcript": "ENST00000645081.1",
          "protein_id": "ENSP00000495540.1",
          "transcript_support_level": null,
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          "cds_start": 527,
          "cds_end": null,
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          "cdna_start": 1642,
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          "cdna_length": 4773,
          "mane_select": null,
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        },
        {
          "aa_ref": "S",
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          "strand": false,
          "consequences": [
            "stop_gained"
          ],
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1427C>A",
          "hgvs_p": "p.Ser476*",
          "transcript": "XM_011528747.3",
          "protein_id": "XP_011527049.2",
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1238C>A",
          "hgvs_p": "p.Ser413*",
          "transcript": "XM_011528748.3",
          "protein_id": "XP_011527050.1",
          "transcript_support_level": null,
          "aa_start": 413,
          "aa_end": null,
          "aa_length": 1111,
          "cds_start": 1238,
          "cds_end": null,
          "cds_length": 3336,
          "cdna_start": 1812,
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          "cdna_length": 6397,
          "mane_select": null,
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        },
        {
          "aa_ref": "S",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "XM_047440075.1",
          "protein_id": "XP_047296031.1",
          "transcript_support_level": null,
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          "cdna_start": 2903,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "S",
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          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
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          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "XM_047440076.1",
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          "cdna_start": 2987,
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          "cdna_length": 7572,
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        },
        {
          "aa_ref": "S",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*",
          "transcript": "XM_047440077.1",
          "protein_id": "XP_047296033.1",
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          "cdna_length": 6715,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "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": "ADNP",
          "gene_hgnc_id": 15766,
          "hgvs_c": "c.202-3546C>A",
          "hgvs_p": null,
          "transcript": "ENST00000644386.1",
          "protein_id": "ENSP00000493755.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 111,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 336,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1198,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ADNP",
      "gene_hgnc_id": 15766,
      "dbsnp": "rs587777524",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.3199999928474426,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.32,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 6.358,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.01,
      "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": 11,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5",
      "acmg_by_gene": [
        {
          "score": 11,
          "benign_score": 0,
          "pathogenic_score": 11,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000621696.5",
          "gene_symbol": "ADNP",
          "hgnc_id": 15766,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AD,Unknown",
          "hgvs_c": "c.1211C>A",
          "hgvs_p": "p.Ser404*"
        }
      ],
      "clinvar_disease": "ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}