The UMD-MSH2 mutations database
Record ID: 945

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.367_645delp.Ala123_Gln215del

wt codonwt aamutant codonmutant aamutational eventmutation type
GCTAladel279aInFIn frame delInF

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding 

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
25_13130_P13130_1_KPE6Relative

Clinical data


Symptom

Reference


Reference IDReference
25Unpublished data