The UMD-MSH2 mutations database
Record ID: 71

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2106_2135delp.Ser703_Val712del

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValdel30cInFIn frame delInF

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
2_PLP-HEGP EXT57_15605_15Relative

Clinical data


Symptom

Reference


Reference IDReference
2Unpublished data