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LOVD - Variant listings for MSH6

About this overview [Show]

Patient data (#0000297)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 9
DNA change c.3851C>T   (View in UCSC Genome Browser)
RNA change r.(?)
Protein p.(Thr1284Met)
MAPP/PP2 Prior P 0.935
Prior P 0.900
IARC Classification Class 3: Uncertain
InSiGHT Classification Class 3: Uncertain
Tumour Char LR 0.100
Segregation LR -
Odds for causality 0.100
Posterior P 0.4737
Reference Thompson et al., 2014, InSiGHT
Variant remarks -
Template DNA
Technique SEQ
DB-ID MSH6_00040

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 9 c.3851C>T r.(?) p.(Thr1284Met) 0.935 0.900 Class 3: Uncertain Class 3: Uncertain 0.100 - 0.100 0.4737 Thompson et al., 2014, InSiGHT - DNA SEQ MSH6_00040