S37P (p.Ser37Pro) variant of SMAD3 (SMAD family member 3)
S37P (p.Ser37Pro) in SMAD3 (SMAD family member 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data, published literature, and structural context.
S37P (p.Ser37Pro) variant details
- p.Ser37Pro
- gnomAD 15-67098949-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.64
- CADD 11.30
- Most common in the Non-Finnish European population (allele frequency 3.2e-06)
- Structural context available
- Literature evidence available