The UMD-MSH2 mutations database
Record ID: 3170

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.439_440delGTp.Val147CysfsX4

wt codonwt aamutant codonmutant aamutational eventmutation type
GTTValdel2aFs.Stop at 150Fr.

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_Ni1401347995261Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data