P10S (p.Pro10Ser) variant of HNRNPA1 (P09651)
P10S (p.Pro10Ser) in HNRNPA1 (P09651) 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 0.62 / 1. The record also includes population frequency data and structural context.
P10S (p.Pro10Ser) variant details
- p.Pro10Ser
- NCI-TCGA Cosmic COSV9926
- cosmic curated COSV99267
- gnomAD rs1944167744
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.625
- REVEL 0.59
- CADD 24.70
- PolyPhen-2 0.75
- SIFT 0.08
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available