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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0026737)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 7
DNA change c.1249_1251dup
RNA change r.(?)
Protein p.(Val417dup)
MAPP/PP2 Prior P 0.893
Prior P 0.893
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR 6.96
Segregation LR 7.423
Odds for causality 51.67
Posterior P 0.9952
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 7 c.1249_1251dup r.(?) p.(Val417dup) 0.893 0.893 Class 5: Pathogenic Class 5: Pathogenic 6.96 7.423 51.67 0.9952 InSiGHT - DNA SEQ