P56T (p.Pro56Thr) variant of ID3 (Q02535)
P56T (p.Pro56Thr) in ID3 (Q02535) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P56T (p.Pro56Thr) variant details
- p.Pro56Thr
- NCI-TCGA Cosmic COSV6580
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available