S14F (p.Ser14Phe) variant of CLDN10 (Claudin-10)
S14F (p.Ser14Phe) in CLDN10 (Claudin-10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data, published literature, and structural context.
S14F (p.Ser14Phe) variant details
- p.Ser14Phe
- rs1377754819
- gnomAD 13-95433865-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.671
- CADD 11.80
- Population evidence available
- Structural context available
- Literature evidence available