G42C (p.Gly42Cys) variant of MAPT (P10636)
G42C (p.Gly42Cys) 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.
G42C (p.Gly42Cys) variant details
- p.Gly42Cys
- NCI-TCGA Cosmic COSV9929
- cosmic curated COSV99290
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available