The UMD-MSH2 mutations database
Record ID: 2966

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.401_402insCAp.Leu135IlefsX40

wt codonwt aamutant codonmutant aamutational eventmutation type
ATTIleins2cFs.Stop at 174

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
4_10322255613382Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data