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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0000253)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 5i
DNA change c.942+3A>T   (View in UCSC Genome Browser)
RNA change r.793_942del
Protein p.Val265_Gln314del
MAPP/PP2 Prior P -
Prior P 0.260
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR -
Segregation LR 2.09E+04
Odds for causality 2.09E+04
Posterior P 0.9999
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 5i c.942+3A>T r.793_942del p.Val265_Gln314del - 0.260 Class 5: Pathogenic Class 5: Pathogenic - 2.09E+04 2.09E+04 0.9999 Thompson et al., 2013 - DNA SEQ