Q14S (p.Gln14Ser) variant of CLCN5 (P51795)
Q14S (p.Gln14Ser) in CLCN5 (P51795) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
Q14S (p.Gln14Ser) variant details
- p.Gln14Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available