N28N (p.Asn28Asn) variant of CHEK1 (O14757)
N28N (p.Asn28Asn) in CHEK1 (O14757) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
N28N (p.Asn28Asn) variant details
- p.Asn28Asn
- rs1057440910
- gnomAD 11-125625838-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0934
- CADD 1.80
- Most common in the African/African-American population (allele frequency 0.0014)
- Structural context available
- Literature evidence available