The UMD-MSH2 mutations database
Record ID: 997

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1980_1981delTAp.Asp660GlufsX15

wt codonwt aamutant codonmutant aamutational eventmutation type
GATAspdel2cFs.Stop at 674Fr.

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_H367_H367-1_H367-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data