T72A (p.Thr72Ala) variant of SMAD2 (SMAD family member 2)
T72A (p.Thr72Ala) in SMAD2 (SMAD family member 2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T72A (p.Thr72Ala) variant details
- p.Thr72Ala
- NCI-TCGA Cosmic COSV5099
- cosmic curated COSV50992
- TOPMed rs1830929483
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available