P26T (p.Pro26Thr) variant of MYL3 (Myosin light chain 3)
P26T (p.Pro26Thr) in MYL3 (Myosin light chain 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
P26T (p.Pro26Thr) variant details
- p.Pro26Thr
- gnomAD 3-46863315-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.167
- REVEL 0.12
- CADD 6.31
- PolyPhen-2 0.02
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available