The UMD-APC mutations database
Record ID: 2866

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.607C>Gp.Gln203Glu

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnGAAGluC->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
 NoNo

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
0.810.06 (non pathogenous)35 (Polymorphism)

Patient and sample data


Sample IDPatient status
19_18991---18991.001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data