The UMD-MSH6 mutations database
Record ID: 2100

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.973C>Tp.Gln325X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnTAAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
 NoNo

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
8_474129315208-296041Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data