The UMD-MSH2 mutations database
Record ID: 1361

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2191delGp.Glu731LysfsX14

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGludel1aFs.Stop at 744Fr.

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
38_18_A2_1574Relative

Clinical data


Symptom

Reference


Reference IDReference
38Unpublished data