The UMD-MSH2 mutations database
Record ID: 3099

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS10-2A>G (c.1662-2A>G)

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerspl-2Spl.A>G

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

Mutation impact


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

Impact on splicing
Splice site type Wild type sequence CV Mutant type sequence CV Variation (%)
Acceptor
ttcgatttgcagCA
87 _
ttcgatttgcggCA
58 _ *
-33.3 %

Patient and sample data


Sample IDPatient status
19_2711027110-00127110-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data