The UMD-MSH2 mutations database
Record ID: 357

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1337_1338delACp.Asp446ValfsX21

wt codonwt aamutant codonmutant aamutational eventmutation type
GACAspdel2bFs.Stop at 466Fr.

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
6_608341_B00066846_S0632Relative

Clinical data


Symptom

Reference


Reference IDReference
6Unpublished data