The UMD-MSH2 mutations database
Record ID: 66

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2012A>Tp.Asn671Ile

wt codonwt aamutant codonmutant aamutational eventmutation type
AATAsnATTIleA->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 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
2_02-DDM9126_31068_31068Relative

Clinical data


Symptom

Reference


Reference IDReference
2Unpublished data