The UMD-MSH2 mutations database
Record ID: 173

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1511_1661delp.Gly504AlafsX3

wt codonwt aamutant codonmutant aamutational eventmutation type
GGCGlydel151bFs.Stop at 506Fr.

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
4_H07064_20389_2051Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data