M6N (p.Met6Asn) variant of WAS (P42768)
M6N (p.Met6Asn) in WAS (P42768) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
M6N (p.Met6Asn) variant details
- p.Met6Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available