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LOVD - Variant listings for MSH2

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Patient data (#0026729)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Probably no pathogenicity
Concluded pathogenicity Probably no pathogenicity
Exon 12
DNA change c.1963G>A
RNA change r.(?)
Protein p.(Val655Ile)
MAPP/PP2 Prior P 0.000452
Prior P 0.1
IARC Classification Class 2: Likely not pathogenic
InSiGHT Classification Class 2: Likely not pathogenic
Tumour Char LR 0.08
Segregation LR -
Odds for causality 0.08
Posterior P 0.0088
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 12 c.1963G>A r.(?) p.(Val655Ile) 0.000452 0.1 Class 2: Likely not pathogenic Class 2: Likely not pathogenic 0.08 - 0.08 0.0088 InSiGHT - DNA SEQ