The UMD-MSH2 mutations database
Record ID: 2253

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2579_2592delp.Ser860TyrfsX17

wt codonwt aamutant codonmutant aamutational eventmutation type
TCGSerdel14bFs.Stop at 876Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Helix-turn-helix 

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
7_1313014583E111688Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data