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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0026739)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 3
DNA change c.599T>A
RNA change r.(?)
Protein p.(Val200Asp)
MAPP/PP2 Prior P 0.915403
Prior P 0.9
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR 23.56
Segregation LR 1.985
Odds for causality 46.78
Posterior P 0.9976
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.599T>A r.(?) p.(Val200Asp) 0.915403 0.9 Class 5: Pathogenic Class 5: Pathogenic 23.56 1.985 46.78 0.9976 InSiGHT - DNA SEQ