P6S (p.Pro6Ser) variant of HAVCR2 (Q8TDQ0)
P6S (p.Pro6Ser) in HAVCR2 (Q8TDQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P6S (p.Pro6Ser) variant details
- p.Pro6Ser
- NCI-TCGA Cosmic COSV5715
- cosmic curated COSV57152
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.