The UMD-MSH2 mutations database
Record ID: 712

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1662_2805delp.Ser554_Met592delinsArg

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerdel1144cFs.In frame delFr.

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
19_4146_4146-003_4146-003Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data