The UMD-MSH2 mutations database
Record ID: 2221

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2580G>Ap.Ser860Ser

wt codonwt aamutant codonmutant aamutational eventmutation type
TCGSerTCASerG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Helix-turn-helix NoYes

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)
0.930.76 (non pathogenous)18 (Polymorphism)

Patient and sample data


Sample IDPatient status
7_85728848E080628Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data