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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0000244)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 3
DNA change c.561_569del
RNA change r.(?)
Protein p.(Glu188_Leu190del)
MAPP/PP2 Prior P -
Prior P 0.900
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR -
Segregation LR 86.723
Odds for causality 86.723
Posterior P 0.9987
Reference InSiGHT
Variant remarks -
Template DNA
Technique SEQ

1 entry in MSH2

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
MAPP/PP2 Prior P Descending
Ascending
Prior P Descending
Ascending
IARC Classification Descending
Ascending
InSiGHT Classification Descending
Ascending
Tumour Char LR Descending
Ascending
Segregation LR Descending
Ascending
Odds for causality Descending
Ascending
Posterior P Descending
Ascending
Reference Descending
Ascending
Variant remarks Descending
Ascending
Template Descending
Ascending
Technique Descending
Ascending
+/+ Unknown 3 c.561_569del r.(?) p.(Glu188_Leu190del) - 0.900 Class 5: Pathogenic Class 5: Pathogenic - 86.723 86.723 0.9987 InSiGHT - DNA SEQ