P74A (p.Pro74Ala) variant of MYL2 (P10916)
P74A (p.Pro74Ala) in MYL2 (P10916) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
P74A (p.Pro74Ala) variant details
- p.Pro74Ala
- gnomAD 12-110914300-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- CADD 7.74
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available
- Literature evidence available