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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0000161)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity No known pathogenicity
Concluded pathogenicity No known pathogenicity
Exon 3'UTR
DNA change c.*129T>C   (View in UCSC Genome Browser)
RNA change r.(?)
Protein p.(=)
MAPP/PP2 Prior P -
Prior P 0.260
IARC Classification Class 1: Not pathogenic
InSiGHT Classification Class 1: Not pathogenic
Tumour Char LR 0.003
Segregation LR 0.793
Odds for causality 0.002
Posterior P 0.0008
Reference Thompson et al., 2013
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'UTR c.*129T>C r.(?) p.(=) - 0.260 Class 1: Not pathogenic Class 1: Not pathogenic 0.003 0.793 0.002 0.0008 Thompson et al., 2013 - DNA SEQ