The UMD-MSH2 mutations database
Record ID: 823

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.528_529delTGp.Cys176X

wt codonwt aamutant codonmutant aamutational eventmutation type
TGTCysdel2cFs.Stop at 176Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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_6406_6406-002_6406-002Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data