S29G (p.Ser29Gly) variant of CSRP3 (P50461)
S29G (p.Ser29Gly) in CSRP3 (P50461) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data and structural context.
S29G (p.Ser29Gly) variant details
- p.Ser29Gly
- ExAC rs765951170
- TOPMed rs765951170
- gnomAD rs765951170
- Missense
- Variant Prioritization Score for Impact Estimate 0.683
- REVEL 0.69
- CADD 31.00
- PolyPhen-2 0.91
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available