The UMD-MSH2 mutations database
Record ID: 2942

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1613delAp.Asn538ThrfsX5

wt codonwt aamutant codonmutant aamutational eventmutation type
AACAsndel1bFs.Stop at 542Fr.

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
31_H1290H1290-1H1290-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data