The UMD-MSH2 mutations database
Record ID: 1305

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.390_391delGTp.Gln130HisfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlndel2cFs.Stop at 131Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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
37_L06.31_3258_43853Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data