P39P (p.Pro39Pro) variant of SDHD (O14521)
P39P (p.Pro39Pro) in SDHD (O14521) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
P39P (p.Pro39Pro) variant details
- p.Pro39Pro
- gnomAD 11-112087921-T-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.129
- CADD 6.79
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available