The UMD-MSH2 mutations database
Record ID: 873

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.925delGp.Ala309ProfsX22

wt codonwt aamutant codonmutant aamutational eventmutation type
GCCAladel1aFs.Stop at 330Fr.

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_11668_11668-001_11668-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data