The UMD-MSH2 mutations database
Record ID: 3002

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1463delTp.Leu488TrpfsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
TTGLeudel1bFs.Stop at 496Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Clamp 

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_2468124681.00124681.001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data