A66S (p.Ala66Ser) variant of MAPT (P10636)
A66S (p.Ala66Ser) in MAPT (P10636) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A66S (p.Ala66Ser) variant details
- p.Ala66Ser
- NCI-TCGA Cosmic COSV5224
- cosmic curated COSV52244
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available