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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0000215)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity No known pathogenicity
Concluded pathogenicity No known pathogenicity
Exon 1
DNA change c.23C>T   (View in UCSC Genome Browser)
RNA change r.23c>u
Protein p.Thr8Met
MAPP/PP2 Prior P 0.001
Prior P 0.100
IARC Classification Class 1: Not pathogenic
InSiGHT Classification Class 1: Not pathogenic
Tumour Char LR 0.001
Segregation LR 0.113
Odds for causality 1.13E-04
Posterior P 1.26E-05
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 1 c.23C>T r.23c>u p.Thr8Met 0.001 0.100 Class 1: Not pathogenic Class 1: Not pathogenic 0.001 0.113 1.13E-04 1.26E-05 Thompson et al., 2014, InSiGHT - DNA SEQ