The UMD-MSH2 mutations database
Record ID: 1007

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2106dupp.Ser703ValfsX14

wt codonwt aamutant codonmutant aamutational eventmutation type
TCCSerins1aFs.Stop at 716

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Patient and sample data


Sample IDPatient status
31_H722_H722-1_H722-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data