The UMD-MSH2 mutations database
Record ID: 1014

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2375delAp.Asn792IlefsX20

wt codonwt aamutant codonmutant aamutational eventmutation type
AATAsndel1bFs.Stop at 811Fr.

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
31_H812_H812-1_H812-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data