R9W (p.Arg9Trp) variant of CLN3 (Battenin)
R9W (p.Arg9Trp) in CLN3 (Battenin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
R9W (p.Arg9Trp) variant details
- p.Arg9Trp
- NCI-TCGA Cosmic COSV6048
- cosmic curated COSV60489
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.