A17G (p.Ala17Gly) variant of CDKN1A (P38936)
A17G (p.Ala17Gly) in CDKN1A (P38936) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and published literature.
A17G (p.Ala17Gly) variant details
- p.Ala17Gly
- gnomAD 22-46248220-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.385
- REVEL 0.23
- MetaLR 0.23
- MetaSVM -0.55
- CADD 32.00
- PolyPhen-2 0.66
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Literature evidence available