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LOVD - Variant listings for MSH6

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Patient data (#0000267)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 4
DNA change c.1565A>G   (View in UCSC Genome Browser)
RNA change r.(?)
Protein p.(Gln522Arg)
MAPP/PP2 Prior P 0.003
Prior P 0.100
IARC Classification Class 3: Uncertain
InSiGHT Classification Class 3: Uncertain
Tumour Char LR 6.960
Segregation LR 1.767
Odds for causality 12.300
Posterior P 0.5775
Reference Thompson et al., 2014, InSiGHT
Variant remarks -
Template DNA
Technique SEQ
DB-ID MSH6_00010

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.1565A>G r.(?) p.(Gln522Arg) 0.003 0.100 Class 3: Uncertain Class 3: Uncertain 6.960 1.767 12.300 0.5775 Thompson et al., 2014, InSiGHT - DNA SEQ MSH6_00010