The UMD-MSH6 mutations database
Record ID: 283

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.261_3556delp.Ser87ArgfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
AGTSerdel3296cFs.Stop at 88Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

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_9391_9391-001_9391-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data