The UMD-MSH2 mutations database
Record ID: 800

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.367_1759delp.Ser124MetfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
GCTAladel1393aFs.Stop at 125Fr.

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
19_7084_7084-001_7084-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data