S31N (p.Ser31Asn) variant of CDKN1A (P38936)
S31N (p.Ser31Asn) in CDKN1A (P38936) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and published literature.
S31N (p.Ser31Asn) variant details
- p.Ser31Asn
- gnomAD 22-46247207-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.18
- MetaLR 0.20
- MetaSVM -0.60
- CADD 24.60
- PolyPhen-2 0.67
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Literature evidence available