A13P (p.Ala13Pro) variant of CD3D (P04234)
A13P (p.Ala13Pro) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
A13P (p.Ala13Pro) variant details
- p.Ala13Pro
- gnomAD rs775716265
- Missense
- Variant Prioritization Score for Impact Estimate 0.39
- REVEL 0.33
- CADD 16.20
- PolyPhen-2 0.01
- SIFT 0.10
- Most common in the HGDP:BURUSHO population (allele frequency 0.042)
- Structural context available