The UMD-MSH2 mutations database
Record ID: 185

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.187delGp.Val63X

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValdel1aFs.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
4_Gr2007-28_24705_3090Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data