The UMD-MSH2 mutations database
Record ID: 2619

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.380A>Gp.Asn127Ser

wt codonwt aamutant codonmutant aamutational eventmutation type
AATAsnAGTSerA->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)
0.960.00 (pathogenous)65 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
SO_-4075---G06838Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data