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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0026740)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Probably pathogenic
Exon 9
DNA change c.1409T>G
RNA change r.(?)
Protein p.(Val470Gly)
MAPP/PP2 Prior P 0.725657
Prior P 0.726
IARC Classification Class 4: Likely pathogenic
InSiGHT Classification Class 4: Likely pathogenic
Tumour Char LR 12.81
Segregation LR -
Odds for causality 12.81
Posterior P 0.971
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 9 c.1409T>G r.(?) p.(Val470Gly) 0.725657 0.726 Class 4: Likely pathogenic Class 4: Likely pathogenic 12.81 - 12.81 0.971 InSiGHT - DNA SEQ