Batch queries can be done using pipe "|" as a separator between search terms.
LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0026730)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 13
DNA change c.2023A>G
RNA change r.(?)
Protein p.(Lys675Glu)
MAPP/PP2 Prior P 0.904273
Prior P 0.9
IARC Classification Class 5: Pathogenic
InSiGHT Classification Class 5: Pathogenic
Tumour Char LR 8.66
Segregation LR 2.05
Odds for causality 17.74
Posterior P 0.9938
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 13 c.2023A>G r.(?) p.(Lys675Glu) 0.904273 0.9 Class 5: Pathogenic Class 5: Pathogenic 8.66 2.05 17.74 0.9938 InSiGHT - DNA SEQ