A138T (p.Ala138Thr) variant of RPA1 (P27694)
A138T (p.Ala138Thr) in RPA1 (P27694) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
A138T (p.Ala138Thr) variant details
- p.Ala138Thr
- NCI-TCGA Cosmic COSV5461
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.