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LOVD - Variant listings for MSH2

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Patient data (#0000180)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 10
DNA change c.1571G>T
RNA change r.(?)
Protein p.(Arg524Leu)
MAPP/PP2 Prior P 0.852
Prior P 0.852
IARC Classification Class 3: Uncertain
InSiGHT Classification Class 3: Uncertain
Tumour Char LR 0.1
Segregation LR 3.718
Odds for causality 0.3718
Posterior P 0.681
Reference 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 10 c.1571G>T r.(?) p.(Arg524Leu) 0.852 0.852 Class 3: Uncertain Class 3: Uncertain 0.1 3.718 0.3718 0.681 InSiGHT - DNA SEQ