Description
The PLEC p.Thr4495_Arg4498dup 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: rs782613077) with unknown clinical significance. The variant was identified in control databases in 3 of 208692 chromosomes at a frequency of 0.000014 (Genome Aggregation Database Feb 27, 2017). The variant was observed in the following populations: Latino in 2 of 31860 chromosomes (freq: 0.000063) and South Asian in 1 of 29326 chromosomes (freq: 0.000034); it was not observed in the African, Ashkenazi Jewish, East Asian, European (Finnish), European (non-Finnish) or Other populations. The variant occurs outside of the splicing consensus sequence and in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer) do not predict a difference in splicing. This variant is an in-frame insertion resulting in a duplication between the residues Thr4495 and Arg4498; the impact of this alteration on the PLEC protein function is not known. This duplication occurs in a plectin repeat region at the end of the protein and therefore it is possible that the variation will not have an effect on the protein function. 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 |
