The UMD-MSH2 mutations database
Record ID: 913

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2261delCp.Thr754IlefsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
ACTThrdel1bFs.Stop at 762Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 

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
20_20-4326_---_4326-01Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data