L37M (p.Leu37Met) variant of C2CD2L (O14523)
L37M (p.Leu37Met) in C2CD2L (O14523) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
L37M (p.Leu37Met) variant details
- p.Leu37Met
- gnomAD 11-119107850-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.25
- REVEL 0.06
- ESM-1b 0.71
- AlphaMissense 0.16
- CADD 24.10
- PolyPhen-2 0.63
- SIFT 0.07
- Population evidence available
- Structural context available
- Literature evidence available