The UMD-MSH6 mutations database
Record ID: 2089

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1573A>Gp.Ser525Gly

wt codonwt aamutant codonmutant aamutational eventmutation type
AGTSerGGTGlyA->GTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector Yes, non coding strandNo

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
0.991.00 (non pathogenous)35 (Polymorphism)

Patient and sample data


Sample IDPatient status
19_2746127461-00127461-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data