The UMD-APC mutations database
Record ID: 2386

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.637C>Tp.Arg213X

wt codonwt aamutant codonmutant aamutational eventmutation type
CGAArgTGAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
 NoYes

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
4_1215---4800Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data