L37S (p.Leu37Ser) variant of C2CD2L (O14523)
L37S (p.Leu37Ser) in C2CD2L (O14523) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
L37S (p.Leu37Ser) variant details
- p.Leu37Ser
- gnomAD 11-119107851-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.196
- REVEL 0.07
- ESM-1b 0.10
- AlphaMissense 0.27
- CADD 24.50
- PolyPhen-2 0.53
- SIFT 0.16
- Population evidence available
- Structural context available
- Literature evidence available