T34A (p.Thr34Ala) variant of MYL2 (P10916)
T34A (p.Thr34Ala) in MYL2 (P10916) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
T34A (p.Thr34Ala) variant details
- p.Thr34Ala
- rs745773458
- gnomAD 12-110914297-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- CADD 6.23
- SIFT 1.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available