T33del (p.Thr33del) variant of SDHC (Q99643)
T33del (p.Thr33del) in SDHC (Q99643) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, published literature, and structural context.
T33del (p.Thr33del) variant details
- gnomAD 1-161328411-AACC-
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.355
- CADD 21.20
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available