S41G (p.Ser41Gly) variant of SETD5 (Q9C0A6)
S41G (p.Ser41Gly) in SETD5 (Q9C0A6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data, published literature, and structural context.
S41G (p.Ser41Gly) variant details
- p.Ser41Gly
- gnomAD 3-9429934-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.6
- CADD 21.90
- Most common in the Non-Finnish European population (allele frequency 1.1e-06)
- Structural context available
- Literature evidence available