The UMD-MSH2 mutations database
Record ID: 786

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.260_264delCTTTTp.Ser87CysfsX11

wt codonwt aamutant codonmutant aamutational eventmutation type
TCTSerdel5bFs.Stop at 97Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch 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_6918_6918-001_6918-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data