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LOVD - Variant listings for MSH2

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Patient data (#0000194)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 12
DNA change c.1865C>T   (View in UCSC Genome Browser)
RNA change r.1865c>u
Protein p.Pro622Leu
MAPP/PP2 Prior P 0.927
Prior P 0.900
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR 75.000
Segregation LR 6.71E+04
Odds for causality 75.000
Posterior P 0.9985
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 12 c.1865C>T r.1865c>u p.Pro622Leu 0.927 0.900 Class 5: Pathogenic Class 5: Pathogenic 75.000 6.71E+04 75.000 0.9985 Thompson et al., 2013 - DNA SEQ