P21S (p.Pro21Ser) variant of HNF4A (P41235)
P21S (p.Pro21Ser) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data, published literature, and structural context.
P21S (p.Pro21Ser) variant details
- p.Pro21Ser
- gnomAD 20-44355835-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- CADD 21.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available