The UMD-MSH2 mutations database
Record ID: 3168

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.388_389delCAp.Gln130ValfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlndel2aFs.Stop at 131Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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
37_L99.0726528155797Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data