P110S (p.Pro110Ser) variant of SFTPB (P07988)
P110S (p.Pro110Ser) in SFTPB (P07988) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
P110S (p.Pro110Ser) variant details
- p.Pro110Ser
- NCI-TCGA Cosmic COSV6089
- cosmic curated COSV60892
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.252
- REVEL 0.10
- CADD 16.20
- PolyPhen-2 0.07
- SIFT 0.17
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available