The UMD-MSH2 mutations database
Record ID: 632

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1077_1386dupp.Val463IlefsX29

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValins310aFs.Stop at 491Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Clamp 

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_7199_7199-001_7199-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data