← Back to variant description

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: 3-47017186-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=47017186&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 47017186,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_014159.7",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7602G>A",
          "hgvs_p": "p.Glu2534Glu",
          "transcript": "NM_014159.7",
          "protein_id": "NP_054878.5",
          "transcript_support_level": null,
          "aa_start": 2534,
          "aa_end": null,
          "aa_length": 2564,
          "cds_start": 7602,
          "cds_end": null,
          "cds_length": 7695,
          "cdna_start": 7791,
          "cdna_end": null,
          "cdna_length": 8541,
          "mane_select": "ENST00000409792.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7602G>A",
          "hgvs_p": "p.Glu2534Glu",
          "transcript": "ENST00000409792.4",
          "protein_id": "ENSP00000386759.3",
          "transcript_support_level": 5,
          "aa_start": 2534,
          "aa_end": null,
          "aa_length": 2564,
          "cds_start": 7602,
          "cds_end": null,
          "cds_length": 7695,
          "cdna_start": 7791,
          "cdna_end": null,
          "cdna_length": 8541,
          "mane_select": "NM_014159.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*3325G>A",
          "hgvs_p": null,
          "transcript": "ENST00000330022.11",
          "protein_id": "ENSP00000332415.7",
          "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": 8172,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*3325G>A",
          "hgvs_p": null,
          "transcript": "ENST00000330022.11",
          "protein_id": "ENSP00000332415.7",
          "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": 8172,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7470G>A",
          "hgvs_p": "p.Glu2490Glu",
          "transcript": "NM_001349370.3",
          "protein_id": "NP_001336299.1",
          "transcript_support_level": null,
          "aa_start": 2490,
          "aa_end": null,
          "aa_length": 2520,
          "cds_start": 7470,
          "cds_end": null,
          "cds_length": 7563,
          "cdna_start": 7775,
          "cdna_end": null,
          "cdna_length": 8525,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7470G>A",
          "hgvs_p": "p.Glu2490Glu",
          "transcript": "ENST00000638947.2",
          "protein_id": "ENSP00000491413.2",
          "transcript_support_level": 5,
          "aa_start": 2490,
          "aa_end": null,
          "aa_length": 2520,
          "cds_start": 7470,
          "cds_end": null,
          "cds_length": 7563,
          "cdna_start": 7544,
          "cdna_end": null,
          "cdna_length": 8302,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7368G>A",
          "hgvs_p": "p.Glu2456Glu",
          "transcript": "ENST00000685005.1",
          "protein_id": "ENSP00000509568.1",
          "transcript_support_level": null,
          "aa_start": 2456,
          "aa_end": null,
          "aa_length": 2486,
          "cds_start": 7368,
          "cds_end": null,
          "cds_length": 7461,
          "cdna_start": 7368,
          "cdna_end": null,
          "cdna_length": 8109,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.4317G>A",
          "hgvs_p": "p.Glu1439Glu",
          "transcript": "ENST00000686876.1",
          "protein_id": "ENSP00000509591.1",
          "transcript_support_level": null,
          "aa_start": 1439,
          "aa_end": null,
          "aa_length": 1469,
          "cds_start": 4317,
          "cds_end": null,
          "cds_length": 4410,
          "cdna_start": 4318,
          "cdna_end": null,
          "cdna_length": 5076,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.3954G>A",
          "hgvs_p": "p.Glu1318Glu",
          "transcript": "ENST00000690157.1",
          "protein_id": "ENSP00000509438.1",
          "transcript_support_level": null,
          "aa_start": 1318,
          "aa_end": null,
          "aa_length": 1348,
          "cds_start": 3954,
          "cds_end": null,
          "cds_length": 4047,
          "cdna_start": 3955,
          "cdna_end": null,
          "cdna_length": 4696,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.3396G>A",
          "hgvs_p": "p.Glu1132Glu",
          "transcript": "ENST00000691902.1",
          "protein_id": "ENSP00000510234.1",
          "transcript_support_level": null,
          "aa_start": 1132,
          "aa_end": null,
          "aa_length": 1162,
          "cds_start": 3396,
          "cds_end": null,
          "cds_length": 3489,
          "cdna_start": 3397,
          "cdna_end": null,
          "cdna_length": 4138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.2658G>A",
          "hgvs_p": "p.Glu886Glu",
          "transcript": "ENST00000691544.1",
          "protein_id": "ENSP00000510710.1",
          "transcript_support_level": null,
          "aa_start": 886,
          "aa_end": null,
          "aa_length": 916,
          "cds_start": 2658,
          "cds_end": null,
          "cds_length": 2751,
          "cdna_start": 2658,
          "cdna_end": null,
          "cdna_length": 3416,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7470G>A",
          "hgvs_p": "p.Glu2490Glu",
          "transcript": "XM_047448045.1",
          "protein_id": "XP_047304001.1",
          "transcript_support_level": null,
          "aa_start": 2490,
          "aa_end": null,
          "aa_length": 2520,
          "cds_start": 7470,
          "cds_end": null,
          "cds_length": 7563,
          "cdna_start": 7572,
          "cdna_end": null,
          "cdna_length": 8322,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7335G>A",
          "hgvs_p": "p.Glu2445Glu",
          "transcript": "XM_024453487.2",
          "protein_id": "XP_024309255.1",
          "transcript_support_level": null,
          "aa_start": 2445,
          "aa_end": null,
          "aa_length": 2475,
          "cds_start": 7335,
          "cds_end": null,
          "cds_length": 7428,
          "cdna_start": 7437,
          "cdna_end": null,
          "cdna_length": 8187,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7170G>A",
          "hgvs_p": "p.Glu2390Glu",
          "transcript": "XM_024453488.2",
          "protein_id": "XP_024309256.1",
          "transcript_support_level": null,
          "aa_start": 2390,
          "aa_end": null,
          "aa_length": 2420,
          "cds_start": 7170,
          "cds_end": null,
          "cds_length": 7263,
          "cdna_start": 7231,
          "cdna_end": null,
          "cdna_length": 7981,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*2927G>A",
          "hgvs_p": null,
          "transcript": "ENST00000431180.5",
          "protein_id": "ENSP00000388349.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7555,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1552G>A",
          "hgvs_p": null,
          "transcript": "ENST00000445387.5",
          "protein_id": "ENSP00000411901.1",
          "transcript_support_level": 5,
          "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": 7075,
          "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": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.4411G>A",
          "hgvs_p": null,
          "transcript": "ENST00000685237.1",
          "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": 5152,
          "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": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1808G>A",
          "hgvs_p": null,
          "transcript": "ENST00000685505.1",
          "protein_id": "ENSP00000510732.1",
          "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": 6667,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1708G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686773.1",
          "protein_id": "ENSP00000510025.1",
          "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": 6508,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.1824G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686792.1",
          "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": 2565,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.1821G>A",
          "hgvs_p": null,
          "transcript": "ENST00000687657.1",
          "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": 2579,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1378G>A",
          "hgvs_p": null,
          "transcript": "ENST00000688290.1",
          "protein_id": "ENSP00000509825.1",
          "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": 6182,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*457G>A",
          "hgvs_p": null,
          "transcript": "ENST00000690461.1",
          "protein_id": "ENSP00000509352.1",
          "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": 6631,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.3531G>A",
          "hgvs_p": null,
          "transcript": "ENST00000692362.1",
          "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": 4272,
          "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": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1889G>A",
          "hgvs_p": null,
          "transcript": "ENST00000692883.1",
          "protein_id": "ENSP00000510674.1",
          "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": 6748,
          "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": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1804G>A",
          "hgvs_p": null,
          "transcript": "ENST00000693321.1",
          "protein_id": "ENSP00000508996.1",
          "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": 6602,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.3043G>A",
          "hgvs_p": null,
          "transcript": "ENST00000693738.1",
          "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": 3784,
          "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": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.7959G>A",
          "hgvs_p": null,
          "transcript": "NR_146158.3",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8709,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*2927G>A",
          "hgvs_p": null,
          "transcript": "ENST00000431180.5",
          "protein_id": "ENSP00000388349.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7555,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1552G>A",
          "hgvs_p": null,
          "transcript": "ENST00000445387.5",
          "protein_id": "ENSP00000411901.1",
          "transcript_support_level": 5,
          "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": 7075,
          "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": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1808G>A",
          "hgvs_p": null,
          "transcript": "ENST00000685505.1",
          "protein_id": "ENSP00000510732.1",
          "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": 6667,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1708G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686773.1",
          "protein_id": "ENSP00000510025.1",
          "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": 6508,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1378G>A",
          "hgvs_p": null,
          "transcript": "ENST00000688290.1",
          "protein_id": "ENSP00000509825.1",
          "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": 6182,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*457G>A",
          "hgvs_p": null,
          "transcript": "ENST00000690461.1",
          "protein_id": "ENSP00000509352.1",
          "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": 6631,
          "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": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1889G>A",
          "hgvs_p": null,
          "transcript": "ENST00000692883.1",
          "protein_id": "ENSP00000510674.1",
          "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": 6748,
          "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": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1804G>A",
          "hgvs_p": null,
          "transcript": "ENST00000693321.1",
          "protein_id": "ENSP00000508996.1",
          "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": 6602,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "SETD2",
      "gene_hgnc_id": 18420,
      "dbsnp": "rs1248081279",
      "frequency_reference_population": 0.000008054383,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 13,
      "gnomad_exomes_af": 0.0000082087,
      "gnomad_genomes_af": 0.00000657186,
      "gnomad_exomes_ac": 12,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.3700000047683716,
      "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": -0.37,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 4.791,
      "phylop100way_prediction": "Uncertain_significance",
      "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": -8,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Moderate,BS2",
      "acmg_by_gene": [
        {
          "score": -8,
          "benign_score": 8,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Moderate",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_014159.7",
          "gene_symbol": "SETD2",
          "hgnc_id": 18420,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.7602G>A",
          "hgvs_p": "p.Glu2534Glu"
        }
      ],
      "clinvar_disease": "Luscan-Lumish syndrome",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Luscan-Lumish syndrome",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}