P91S (p.Pro91Ser) variant of ABCA1 (O95477)
P91S (p.Pro91Ser) in ABCA1 (O95477) 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 0.86 / 1. The record also includes population frequency data and structural context.
P91S (p.Pro91Ser) variant details
- p.Pro91Ser
- rs1436757527
- NCI-TCGA Cosmic COSV6605
- cosmic curated COSV66058
- gnomAD rs1436757527
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.863
- REVEL 0.89
- MetaLR 1.00
- MetaSVM 0.93
- CADD 26.50
- PolyPhen-2 0.72
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.7e-05)
- Structural context available