The UMD-APC mutations database
Record ID: 4900

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2498delGp.Ser833ThrfsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerdel1bFs.Stop at 841Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

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_-3579G04430G04430Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data