The UMD-MSH2 mutations database
Record ID: 2217

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2251G>Ap.Gly751Arg

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlyAGAArgG->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)
0.990.00 (pathogenous)94 (Pathogenous)

Patient and sample data


Sample IDPatient status
7_5710 (-4307)2839E060912Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data