V39V (p.Val39Val) variant of ETFDH (Q16134)
V39V (p.Val39Val) in ETFDH (Q16134) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
V39V (p.Val39Val) variant details
- p.Val39Val
- rs2150304380
- gnomAD 4-158680549-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.111
- CADD 4.32
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available