The UMD-MSH2 mutations database
Record ID: 466

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.812_813delCTp.Ser271CysfsX12

wt codonwt aamutant codonmutant aamutational eventmutation type
TCTSerdel2bFs.Stop at 282Fr.

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
8_44989_80751_08-417121EGRelative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data