The UMD-MSH2 mutations database
Record ID: 267

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1387_1510delp.Val463AlafsX22

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValdel124aFs.Stop at 484Fr.

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
5_2008320_20083512_AAC692Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data