The UMD-MSH6 mutations database
Record ID: 1969

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.546delCp.Leu183X

wt codonwt aamutant codonmutant aamutational eventmutation type
GCCAladel1cFs.Stop at 183Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
PWWP 

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_H14194335405117Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data