Description
The ERCC5 p.Gln16Gln variant was not identified in the literature nor was it identified in ClinVar, Cosmic or LOVD 3.0. The variant was identified in dbSNP (ID: rs202038276) and in control databases in 24 of 280740 chromosomes (1 homozygous) at a frequency of 0.000085 (Genome Aggregation Database Feb 27, 2017). The variant was observed in the following populations: Ashkenazi Jewish in 23 of 10332 chromosomes (freq: 0.002226) and European (non-Finnish) in 1 of 127854 chromosomes (freq: 0.000008); it was not observed in the African, Latino, East Asian, European (Finnish), Other and South Asian populations. The p.Gln16Gln variant is not expected to have clinical significance because it does not result in a change of amino acid (synonymous change) and is not located in a known consensus splice site. However, 4 of 4 in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer) predict the loss of both a 5' and 3' splice site at the variant location, although neither of these are known splice sites. This information is not predictive enough to assume pathogenicity. In summary, based on the above information the clinical significance of this variant cannot be determined with certainty at this time. This variant is classified as a variant of uncertain significance.
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | unknown | yes | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
