P51S (p.Pro51Ser) variant of HNF4A (P41235)
P51S (p.Pro51Ser) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data, published literature, and structural context.
P51S (p.Pro51Ser) variant details
- p.Pro51Ser
- rs1489609624
- gnomAD 20-44402563-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.219
- CADD 2.96
- Most common in the South Asian population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available