T6T (p.Thr6Thr) variant of HNF4A (P41235)
T6T (p.Thr6Thr) in HNF4A (P41235) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
T6T (p.Thr6Thr) variant details
- p.Thr6Thr
- gnomAD 20-44401390-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.679
- CADD 9.95
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available