M36I (p.Met36Ile) variant of HNF4A (P41235)
M36I (p.Met36Ile) in HNF4A (P41235) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
M36I (p.Met36Ile) variant details
- p.Met36Ile
- ExAC rs745604501
- TOPMed rs745604501
- gnomAD rs745604501
- Missense
- Variant Prioritization Score for Impact Estimate 0.422
- REVEL 0.19
- MetaLR 0.61
- MetaSVM -0.66
- CADD 22.30
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available