The UMD-MSH2 mutations database
Record ID: 3228

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1674_1677delinsCTTTT

wt codonwt aamutant codonmutant aamutational eventmutation type
TCTSerindelsindelsindelsindels

StructureKey Residue (HCD)Pyrimidin doubletCpG
Lever 

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)
1 - 65 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
19_2772927729-00127729-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data