The UMD-MSH2 mutations database
Record ID: 3083

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1091A>Cp.Glu364Ala

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGluGCAAlaA->CTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Lever 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)
0.990.00 (pathogenous)82 (Pathogenous)

Patient and sample data


Sample IDPatient status
19_2566825668.00125668.001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data