The UMD-MSH2 mutations database
Record ID: 987

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.166delGp.Glu56ArgfsX8

wt codonwt aamutant codonmutant aamutational eventmutation type
GAGGludel1aFs.Stop at 63Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding 

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_H203_H203-2_H203-2ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data