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LOVD - Variant listings for MSH6

About this overview [Show]

Patient data (#0000294)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 8
DNA change c.3674C>T   (View in UCSC Genome Browser)
RNA change r.(?)
Protein p.(Thr1225Met)
MAPP/PP2 Prior P 0.734
Prior P 0.734
IARC Classification Class 3: Uncertain
InSiGHT Classification Class 3: Uncertain
Tumour Char LR 0.100
Segregation LR -
Odds for causality 0.100
Posterior P 0.2159
Reference Thompson et al., 2014, InSiGHT
Variant remarks -
Template DNA
Technique SEQ
DB-ID MSH6_00037

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 8 c.3674C>T r.(?) p.(Thr1225Met) 0.734 0.734 Class 3: Uncertain Class 3: Uncertain 0.100 - 0.100 0.2159 Thompson et al., 2014, InSiGHT - DNA SEQ MSH6_00037