H42G (p.His42Gly) variant of PHF6 (PHD finger protein 6)
H42G (p.His42Gly) in PHF6 (PHD finger protein 6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
H42G (p.His42Gly) variant details
- p.His42Gly
- NCI-TCGA Cosmic COSV5969
- NCI-TCGA Cosmic COSV5970
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available