G21W (p.Gly21Trp) variant of MAPT (P10636)
G21W (p.Gly21Trp) 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.
G21W (p.Gly21Trp) variant details
- p.Gly21Trp
- NCI-TCGA Cosmic COSV5224
- cosmic curated COSV52249
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available