W9R (p.Trp9Arg) variant of SFTPB (P07988)
W9R (p.Trp9Arg) in SFTPB (P07988) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
W9R (p.Trp9Arg) variant details
- p.Trp9Arg
- gnomAD rs1164736987
- Missense
- Variant Prioritization Score for Impact Estimate 0.311
- REVEL 0.26
- CADD 23.10
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available