The UMD-MSH2 mutations database
Record ID: 660

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1277_2805del

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlydel1529bFs.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_8387_8387-001_8387-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data