The UMD-MSH2 mutations database
Record ID: 1029

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.387_388delTCp.Gln130ValfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
TCTSerdel2cFs.Stop at 131Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

Mutation impact


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

Patient and sample data


Sample IDPatient status
31_H211_H211_1_H211_1_ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data