The UMD-MSH2 mutations database
Record ID: 609

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1059delGp.Asn354ThrfsX3

wt codonwt aamutant codonmutant aamutational eventmutation type
AAGLysdel1cFs.Stop at 356Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 

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
19_15855_15855-001_15855-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data