The UMD-MSH2 mutations database
Record ID: 770

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2241delAp.Ile747MetfsX16

wt codonwt aamutant codonmutant aamutational eventmutation type
ATAIledel1cFs.Stop at 762Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 

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_2938_2938-001_2938-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data