Q89R (p.Gln89Arg) variant of SFTPB (P07988)
Q89R (p.Gln89Arg) in SFTPB (P07988) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
Q89R (p.Gln89Arg) variant details
- p.Gln89Arg
- gnomAD rs1677687817
- Missense
- Variant Prioritization Score for Impact Estimate 0.608
- REVEL 0.62
- CADD 32.00
- PolyPhen-2 0.84
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available