The UMD-MSH2 mutations database
Record ID: 3055

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1705_1706delGAp.Glu569IlefsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGludel2aFs.Stop at 570Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Lever 

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
31_H1746H1746-1H1746-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data