S13T (p.Ser13Thr) variant of MYPN (Myopalladin)
S13T (p.Ser13Thr) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
S13T (p.Ser13Thr) variant details
- p.Ser13Thr
- ExAC rs772628299
- TOPMed rs772628299
- gnomAD rs772628299
- Missense
- Variant Prioritization Score for Impact Estimate 0.3
- REVEL 0.09
- CADD 21.90
- PolyPhen-2 0.02
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available