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LOVD - Variant listings for MSH2

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Patient data (#0000251)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 5
DNA change c.929T>C   (View in UCSC Genome Browser)
RNA change r.(?)
Protein p.(Leu310Pro)
MAPP/PP2 Prior P 0.961
Prior P 0.900
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR 6.960
Segregation LR 1.941
Odds for causality 13.511
Posterior P 0.9918
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 5 c.929T>C r.(?) p.(Leu310Pro) 0.961 0.900 Class 5: Pathogenic Class 5: Pathogenic 6.960 1.941 13.511 0.9918 Thompson et al., 2014, InSiGHT - DNA SEQ