The UMD-APC mutations database
Record ID: 2162

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.4598delAp.Asn1533MetfsX32

wt codonwt aamutant codonmutant aamutational eventmutation type
AATAsndel1bFs.Stop at 1564Fr.

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
4_21374---21374Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data