The UMD-MSH2 mutations database
Record ID: 3060

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.135_136delGCp.His46ArgfsX35

wt codonwt aamutant codonmutant aamutational eventmutation type
GCGAladel2cFs.Stop at 80Fr.

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
4_07173225052597Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data