Description
Variant summary: MLH1 c.1808C>G (p.Pro603Arg) results in a non-conservative amino acid change located in the DNA mismatch repair protein Mlh1, C-terminal domain (IPR032189) of the encoded protein sequence. Five of five in-silico tools predict a damaging effect of the variant on protein function. The variant allele was found at a frequency of 0.00016 in 251344 control chromosomes. This frequency is not significantly higher than expected for a pathogenic variant in MLH1 causing Hereditary Nonpolyposis Colorectal Cancer (0.00016 vs 0.00071), allowing no conclusion about variant significance. However, it is predominantly observed in the Ashkenazi Jewish subpopulation at a frequency of 0.0028 (28/10076). This frequency is about 4 times the estimated maximal expected allele frequency of a pathogenic MLH1 variant (0.0007105), suggesting this is likely a benign polymorphism found primarily in the populations of Ashkenazi Jewish origin. c.1808C>G has been reported in the literature in individuals affected with a variety of cancers such as Hereditary Nonpolyposis Colorectal Cancer/Lynch syndrome, epithelial ovarian cancer (example, Hardt_2011, Tournier_2008, Pal_2012). These report(s) do not provide unequivocal conclusions about association of the variant with Hereditary Nonpolyposis Colorectal Cancer/Lynch syndrome. At-least one co-occurrence with another pathogenic variant has been reported in the UMD database (MLH1 complete gene deletion), providing supporting evidence for a benign role. Several publications report experimental evidence evaluating an impact on protein function (example, Takahashi_2007, Drost_2018). The most pronounced variant effect results in 82.5% normal mismatch repair (MMR) activity (Takahashi_2007), while a subsequent study reports 97% of normal mismatch repair (MMR) activity (Drost_2018). Furthermore, binding partner interaction as determined by Y2H assays is +, Nuclear localization as determined by transfections of fluorescently tagged proteins combined with microscopy is + (Drost_2018). Multiple clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation with a predominant consensus as likely benign/benign (n=7) (VUS, n=2). Some submitters cite overlapping evidence utilized in the context of this evaluation. Based on the evidence outlined above, the variant was classified as benign.
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | unknown | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
