P119S (p.Pro119Ser) variant of ASH1L (Q9NR48)
P119S (p.Pro119Ser) in ASH1L (Q9NR48) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P119S (p.Pro119Ser) variant details
- p.Pro119Ser
- NCI-TCGA Cosmic COSV6420
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.