The UMD-MSH2 mutations database
Record ID: 492

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1309delGp.Val437X

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValdel1aFs.Stop at 437Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 

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
17_Paris-F9880_5001117_90Relative

Clinical data


Symptom

Reference


Reference IDReference
17Unpublished data