← 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: 21-46125610-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=46125610&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "21",
      "pos": 46125610,
      "ref": "C",
      "alt": "G",
      "effect": "synonymous_variant",
      "transcript": "NM_001849.4",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "NM_001849.4",
          "protein_id": "NP_001840.3",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000300527.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001849.4"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000300527.9",
          "protein_id": "ENSP00000300527.4",
          "transcript_support_level": 1,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001849.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000300527.9"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "NM_058174.3",
          "protein_id": "NP_478054.2",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 918,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 2757,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": "ENST00000397763.6",
          "biotype": "protein_coding",
          "feature": "NM_058174.3"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000397763.6",
          "protein_id": "ENSP00000380870.1",
          "transcript_support_level": 5,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 918,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 2757,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": "NM_058174.3",
          "biotype": "protein_coding",
          "feature": "ENST00000397763.6"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.2157C>G",
          "hgvs_p": "p.Ser719Ser",
          "transcript": "ENST00000857098.1",
          "protein_id": "ENSP00000527157.1",
          "transcript_support_level": null,
          "aa_start": 719,
          "aa_end": null,
          "aa_length": 1084,
          "cds_start": 2157,
          "cds_end": null,
          "cds_length": 3255,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857098.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.2124C>G",
          "hgvs_p": "p.Ser708Ser",
          "transcript": "ENST00000857103.1",
          "protein_id": "ENSP00000527162.1",
          "transcript_support_level": null,
          "aa_start": 708,
          "aa_end": null,
          "aa_length": 1073,
          "cds_start": 2124,
          "cds_end": null,
          "cds_length": 3222,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857103.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.2079C>G",
          "hgvs_p": "p.Ser693Ser",
          "transcript": "ENST00000857092.1",
          "protein_id": "ENSP00000527151.1",
          "transcript_support_level": null,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 1058,
          "cds_start": 2079,
          "cds_end": null,
          "cds_length": 3177,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857092.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.2031C>G",
          "hgvs_p": "p.Ser677Ser",
          "transcript": "ENST00000857106.1",
          "protein_id": "ENSP00000527165.1",
          "transcript_support_level": null,
          "aa_start": 677,
          "aa_end": null,
          "aa_length": 1042,
          "cds_start": 2031,
          "cds_end": null,
          "cds_length": 3129,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857106.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.2004C>G",
          "hgvs_p": "p.Ser668Ser",
          "transcript": "ENST00000968880.1",
          "protein_id": "ENSP00000638939.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 1033,
          "cds_start": 2004,
          "cds_end": null,
          "cds_length": 3102,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968880.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1992C>G",
          "hgvs_p": "p.Ser664Ser",
          "transcript": "ENST00000857101.1",
          "protein_id": "ENSP00000527160.1",
          "transcript_support_level": null,
          "aa_start": 664,
          "aa_end": null,
          "aa_length": 1029,
          "cds_start": 1992,
          "cds_end": null,
          "cds_length": 3090,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857101.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857090.1",
          "protein_id": "ENSP00000527149.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857090.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857091.1",
          "protein_id": "ENSP00000527150.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857091.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857094.1",
          "protein_id": "ENSP00000527153.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857094.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857096.1",
          "protein_id": "ENSP00000527155.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857096.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857100.1",
          "protein_id": "ENSP00000527159.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857100.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857108.1",
          "protein_id": "ENSP00000527167.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857108.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857109.1",
          "protein_id": "ENSP00000527168.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857109.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000968878.1",
          "protein_id": "ENSP00000638937.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968878.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000968883.1",
          "protein_id": "ENSP00000638942.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968883.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000968884.1",
          "protein_id": "ENSP00000638943.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3060,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968884.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1956C>G",
          "hgvs_p": "p.Ser652Ser",
          "transcript": "ENST00000968879.1",
          "protein_id": "ENSP00000638938.1",
          "transcript_support_level": null,
          "aa_start": 652,
          "aa_end": null,
          "aa_length": 1017,
          "cds_start": 1956,
          "cds_end": null,
          "cds_length": 3054,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968879.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1953C>G",
          "hgvs_p": "p.Ser651Ser",
          "transcript": "ENST00000934972.1",
          "protein_id": "ENSP00000605031.1",
          "transcript_support_level": null,
          "aa_start": 651,
          "aa_end": null,
          "aa_length": 1016,
          "cds_start": 1953,
          "cds_end": null,
          "cds_length": 3051,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934972.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857105.1",
          "protein_id": "ENSP00000527164.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1006,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3021,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857105.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1911C>G",
          "hgvs_p": "p.Ser637Ser",
          "transcript": "ENST00000857102.1",
          "protein_id": "ENSP00000527161.1",
          "transcript_support_level": null,
          "aa_start": 637,
          "aa_end": null,
          "aa_length": 1002,
          "cds_start": 1911,
          "cds_end": null,
          "cds_length": 3009,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857102.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1908C>G",
          "hgvs_p": "p.Ser636Ser",
          "transcript": "ENST00000968882.1",
          "protein_id": "ENSP00000638941.1",
          "transcript_support_level": null,
          "aa_start": 636,
          "aa_end": null,
          "aa_length": 1001,
          "cds_start": 1908,
          "cds_end": null,
          "cds_length": 3006,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968882.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1899C>G",
          "hgvs_p": "p.Ser633Ser",
          "transcript": "ENST00000857093.1",
          "protein_id": "ENSP00000527152.1",
          "transcript_support_level": null,
          "aa_start": 633,
          "aa_end": null,
          "aa_length": 998,
          "cds_start": 1899,
          "cds_end": null,
          "cds_length": 2997,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857093.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1899C>G",
          "hgvs_p": "p.Ser633Ser",
          "transcript": "ENST00000857095.1",
          "protein_id": "ENSP00000527154.1",
          "transcript_support_level": null,
          "aa_start": 633,
          "aa_end": null,
          "aa_length": 998,
          "cds_start": 1899,
          "cds_end": null,
          "cds_length": 2997,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857095.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1899C>G",
          "hgvs_p": "p.Ser633Ser",
          "transcript": "ENST00000857099.1",
          "protein_id": "ENSP00000527158.1",
          "transcript_support_level": null,
          "aa_start": 633,
          "aa_end": null,
          "aa_length": 998,
          "cds_start": 1899,
          "cds_end": null,
          "cds_length": 2997,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857099.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1899C>G",
          "hgvs_p": "p.Ser633Ser",
          "transcript": "ENST00000857107.1",
          "protein_id": "ENSP00000527166.1",
          "transcript_support_level": null,
          "aa_start": 633,
          "aa_end": null,
          "aa_length": 998,
          "cds_start": 1899,
          "cds_end": null,
          "cds_length": 2997,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857107.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1899C>G",
          "hgvs_p": "p.Ser633Ser",
          "transcript": "ENST00000934971.1",
          "protein_id": "ENSP00000605030.1",
          "transcript_support_level": null,
          "aa_start": 633,
          "aa_end": null,
          "aa_length": 998,
          "cds_start": 1899,
          "cds_end": null,
          "cds_length": 2997,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934971.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000857097.1",
          "protein_id": "ENSP00000527156.1",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 899,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 2700,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857097.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1557C>G",
          "hgvs_p": "p.Ser519Ser",
          "transcript": "ENST00000968881.1",
          "protein_id": "ENSP00000638940.1",
          "transcript_support_level": null,
          "aa_start": 519,
          "aa_end": null,
          "aa_length": 884,
          "cds_start": 1557,
          "cds_end": null,
          "cds_length": 2655,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968881.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "NM_058175.3",
          "protein_id": "NP_478055.2",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 828,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 2487,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_058175.3"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser",
          "transcript": "ENST00000409416.6",
          "protein_id": "ENSP00000387115.1",
          "transcript_support_level": 5,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 828,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 2487,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409416.6"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.633C>G",
          "hgvs_p": "p.Ser211Ser",
          "transcript": "ENST00000413758.1",
          "protein_id": "ENSP00000395751.1",
          "transcript_support_level": 3,
          "aa_start": 211,
          "aa_end": null,
          "aa_length": 249,
          "cds_start": 633,
          "cds_end": null,
          "cds_length": 750,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000413758.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "COL6A2",
          "gene_hgnc_id": 2212,
          "hgvs_c": "c.709-354C>G",
          "hgvs_p": null,
          "transcript": "ENST00000857104.1",
          "protein_id": "ENSP00000527163.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 539,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1620,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000857104.1"
        }
      ],
      "gene_symbol": "COL6A2",
      "gene_hgnc_id": 2212,
      "dbsnp": "rs150253422",
      "frequency_reference_population": 6.848677e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84868e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.3700000047683716,
      "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": -6.164,
      "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": -1,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -1,
          "benign_score": 3,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001849.4",
          "gene_symbol": "COL6A2",
          "hgnc_id": 2212,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.1962C>G",
          "hgvs_p": "p.Ser654Ser"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}