The UMD-MSH2 mutations database
Record ID: 1084

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.811_814delTCTGp.Ser271ArgfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
TCTSerdel4aFs.Stop at 272Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 

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
33_TNN 247__03-1124Relative

Clinical data


Symptom

Reference


Reference IDReference
33Unpublished data