The UMD-MSH2 mutations database
Record ID: 2955

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.212_366delp.Ala72PhefsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlydel155bFs.Stop at 80Fr.

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
8_431121473408-521111EGSRelative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data