The UMD-MSH2 mutations database
Record ID: 760

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2055delAp.Ile685MetfsX25

wt codonwt aamutant codonmutant aamutational eventmutation type
ATAIledel1cFs.Stop at 709Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 

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
19_8759_8759-001_8759-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data