D39G (p.Asp39Gly) variant of RNF207 (RING finger protein 207)
D39G (p.Asp39Gly) in RNF207 (RING finger protein 207) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data and structural context.
D39G (p.Asp39Gly) variant details
- p.Asp39Gly
- gnomAD rs1159049015
- Missense
- Variant Prioritization Score for Impact Estimate 0.718
- REVEL 0.80
- CADD 27.90
- PolyPhen-2 0.97
- SIFT 0.07
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available