The UMD-MSH2 mutations database
Record ID: 1037

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.529G>Tp.Glu177X

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGluTAAStopG->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector Yes, non coding strandNo

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
31_H678_H678-1_H678-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data