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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0000210)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 1i
DNA change c.212-1G>A   (View in UCSC Genome Browser)
RNA change r.spl?
Protein p.?
MAPP/PP2 Prior P -
Prior P 0.960
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR 8.660
Segregation LR 1.750
Odds for causality 15.158
Posterior P 0.9973
Reference Thompson et al., 2014, 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 1i c.212-1G>A r.spl? p.? - 0.960 Class 5: Pathogenic Class 5: Pathogenic 8.660 1.750 15.158 0.9973 Thompson et al., 2014, InSiGHT - DNA SEQ