The UMD-MSH2 mutations database
Record ID: 1043

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.746delAp.Lys249ArgfsX5

wt codonwt aamutant codonmutant aamutational eventmutation type
AAGLysdel1bFs.Stop at 253Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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
31_H109_H109_3_H109_3_ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data