V9V (p.Val9Val) variant of SDHC (Q99643)
V9V (p.Val9Val) in SDHC (Q99643) is a synonymous 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.
V9V (p.Val9Val) variant details
- p.Val9Val
- gnomAD 1-161323620-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.221
- CADD 6.78
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available