The UMD-MSH2 mutations database
Record ID: 68

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2075G>Ap.Gly692Glu

wt codonwt aamutant codonmutant aamutational eventmutation type
GGGGlyGAGGluG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase Yes, non coding strandNo

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
10.00 (pathogenous)88 (Pathogenous)

Patient and sample data


Sample IDPatient status
2_02-ACT3084_19426_19426Relative

Clinical data


Symptom

Reference


Reference IDReference
2Unpublished data