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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: 16-5082615-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=5082615&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 5082615,
      "ref": "A",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "ENST00000262374.10",
      "consequences": [
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.1129A>T",
          "hgvs_p": "p.Met377Leu",
          "transcript": "NM_019109.5",
          "protein_id": "NP_061982.3",
          "transcript_support_level": null,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 464,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 1395,
          "cdna_start": 1136,
          "cdna_end": null,
          "cdna_length": 3900,
          "mane_select": "ENST00000262374.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.1129A>T",
          "hgvs_p": "p.Met377Leu",
          "transcript": "ENST00000262374.10",
          "protein_id": "ENSP00000262374.5",
          "transcript_support_level": 1,
          "aa_start": 377,
          "aa_end": null,
          "aa_length": 464,
          "cds_start": 1129,
          "cds_end": null,
          "cds_length": 1395,
          "cdna_start": 1136,
          "cdna_end": null,
          "cdna_length": 3900,
          "mane_select": "NM_019109.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.796A>T",
          "hgvs_p": "p.Met266Leu",
          "transcript": "ENST00000588623.5",
          "protein_id": "ENSP00000468118.1",
          "transcript_support_level": 1,
          "aa_start": 266,
          "aa_end": null,
          "aa_length": 353,
          "cds_start": 796,
          "cds_end": null,
          "cds_length": 1062,
          "cdna_start": 1896,
          "cdna_end": null,
          "cdna_length": 2671,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.*1030A>T",
          "hgvs_p": null,
          "transcript": "ENST00000591822.5",
          "protein_id": "ENSP00000467865.1",
          "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": 1689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.*1030A>T",
          "hgvs_p": null,
          "transcript": "ENST00000591822.5",
          "protein_id": "ENSP00000467865.1",
          "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": 1689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.1090A>T",
          "hgvs_p": "p.Met364Leu",
          "transcript": "NM_001438123.1",
          "protein_id": "NP_001425052.1",
          "transcript_support_level": null,
          "aa_start": 364,
          "aa_end": null,
          "aa_length": 451,
          "cds_start": 1090,
          "cds_end": null,
          "cds_length": 1356,
          "cdna_start": 1097,
          "cdna_end": null,
          "cdna_length": 3861,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.1090A>T",
          "hgvs_p": "p.Met364Leu",
          "transcript": "ENST00000684190.1",
          "protein_id": "ENSP00000507554.1",
          "transcript_support_level": null,
          "aa_start": 364,
          "aa_end": null,
          "aa_length": 451,
          "cds_start": 1090,
          "cds_end": null,
          "cds_length": 1356,
          "cdna_start": 1134,
          "cdna_end": null,
          "cdna_length": 2051,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.1018A>T",
          "hgvs_p": "p.Met340Leu",
          "transcript": "ENST00000684335.1",
          "protein_id": "ENSP00000508112.1",
          "transcript_support_level": null,
          "aa_start": 340,
          "aa_end": null,
          "aa_length": 427,
          "cds_start": 1018,
          "cds_end": null,
          "cds_length": 1284,
          "cdna_start": 1062,
          "cdna_end": null,
          "cdna_length": 1952,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.796A>T",
          "hgvs_p": "p.Met266Leu",
          "transcript": "NM_001330504.2",
          "protein_id": "NP_001317433.1",
          "transcript_support_level": null,
          "aa_start": 266,
          "aa_end": null,
          "aa_length": 353,
          "cds_start": 796,
          "cds_end": null,
          "cds_length": 1062,
          "cdna_start": 977,
          "cdna_end": null,
          "cdna_length": 3741,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.796A>T",
          "hgvs_p": "p.Met266Leu",
          "transcript": "ENST00000544428.1",
          "protein_id": "ENSP00000440019.1",
          "transcript_support_level": 2,
          "aa_start": 266,
          "aa_end": null,
          "aa_length": 353,
          "cds_start": 796,
          "cds_end": null,
          "cds_length": 1062,
          "cdna_start": 977,
          "cdna_end": null,
          "cdna_length": 1419,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.796A>T",
          "hgvs_p": "p.Met266Leu",
          "transcript": "ENST00000683739.1",
          "protein_id": "ENSP00000507002.1",
          "transcript_support_level": null,
          "aa_start": 266,
          "aa_end": null,
          "aa_length": 353,
          "cds_start": 796,
          "cds_end": null,
          "cds_length": 1062,
          "cdna_start": 1123,
          "cdna_end": null,
          "cdna_length": 2058,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.640A>T",
          "hgvs_p": "p.Met214Leu",
          "transcript": "ENST00000682985.1",
          "protein_id": "ENSP00000507598.1",
          "transcript_support_level": null,
          "aa_start": 214,
          "aa_end": null,
          "aa_length": 301,
          "cds_start": 640,
          "cds_end": null,
          "cds_length": 906,
          "cdna_start": 1751,
          "cdna_end": null,
          "cdna_length": 2668,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.601A>T",
          "hgvs_p": "p.Met201Leu",
          "transcript": "ENST00000682327.1",
          "protein_id": "ENSP00000507058.1",
          "transcript_support_level": null,
          "aa_start": 201,
          "aa_end": null,
          "aa_length": 288,
          "cds_start": 601,
          "cds_end": null,
          "cds_length": 867,
          "cdna_start": 1712,
          "cdna_end": null,
          "cdna_length": 3395,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.535A>T",
          "hgvs_p": "p.Met179Leu",
          "transcript": "ENST00000682020.1",
          "protein_id": "ENSP00000508075.1",
          "transcript_support_level": null,
          "aa_start": 179,
          "aa_end": null,
          "aa_length": 266,
          "cds_start": 535,
          "cds_end": null,
          "cds_length": 801,
          "cdna_start": 1602,
          "cdna_end": null,
          "cdna_length": 2519,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "c.388A>T",
          "hgvs_p": "p.Met130Leu",
          "transcript": "ENST00000683433.1",
          "protein_id": "ENSP00000507463.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
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          "cds_start": 388,
          "cds_end": null,
          "cds_length": 654,
          "cdna_start": 1455,
          "cdna_end": null,
          "cdna_length": 2345,
          "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": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.3265A>T",
          "hgvs_p": null,
          "transcript": "ENST00000592793.6",
          "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,
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          "cdna_length": 4182,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.*221A>T",
          "hgvs_p": null,
          "transcript": "ENST00000650085.1",
          "protein_id": "ENSP00000507951.1",
          "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": 2870,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.*224A>T",
          "hgvs_p": null,
          "transcript": "ENST00000682206.1",
          "protein_id": "ENSP00000508285.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 2143,
          "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": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.1177A>T",
          "hgvs_p": null,
          "transcript": "ENST00000682314.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 3047,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.3271A>T",
          "hgvs_p": null,
          "transcript": "ENST00000682349.1",
          "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": 4188,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG1",
          "gene_hgnc_id": 18294,
          "hgvs_c": "n.4097A>T",
          "hgvs_p": null,
          "transcript": "ENST00000682703.1",
          "protein_id": null,
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      "gene_symbol": "ALG1",
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      "computational_score_selected": 0.856638491153717,
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      "computational_source_selected": "MetaRNN",
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      "splice_prediction_selected": "Benign",
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      "bayesdelnoaf_score": 0.2,
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      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0,
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      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
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      "acmg_by_gene": [
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            "PP3_Moderate"
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          "verdict": "Uncertain_significance",
          "transcript": "ENST00000262374.10",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  ],
  "message": null
}