N21N (p.Asn21Asn) variant of MSH6 (DNA mismatch repair protein Msh6)
N21N (p.Asn21Asn) in MSH6 (DNA mismatch repair protein Msh6) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data, published literature, and structural context.
N21N (p.Asn21Asn) variant details
- p.Asn21Asn
- rs876660097
- gnomAD 2-47783296-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.675
- CADD 9.34
- Most common in the Ashkenazi Jewish population (allele frequency 7.7e-05)
- Structural context available
- Literature evidence available