The UMD-APC mutations database
Record ID: 4685

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2932C>Tp.Gln978X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnTAAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
 Yes, coding strandNo

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
SO_-1312G03048G03048Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data