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LOVD - Variant listings for MSH6

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Patient data (#0026741)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Probably pathogenic
Exon 4
DNA change c.1621A>C
RNA change r.(?)
Protein p.(Ser541Arg)
MAPP/PP2 Prior P 0.901407
Prior P 0.9
IARC Classification Class 4: Likely pathogenic
InSiGHT Classification Class 4: Likely pathogenic
Tumour Char LR -
Segregation LR 3.702
Odds for causality 3.702
Posterior P 0.9709
Reference InSiGHT
Variant remarks -
Template DNA
Technique SEQ
DB-ID MSH6_00051

1 entry in MSH6

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
DB-ID Descending
Ascending
+?/+? Unknown 4 c.1621A>C r.(?) p.(Ser541Arg) 0.901407 0.9 Class 4: Likely pathogenic Class 4: Likely pathogenic - 3.702 3.702 0.9709 InSiGHT - DNA SEQ MSH6_00051