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LOVD - Variant listings for MSH2

About this overview [Show]

Patient data (#0000250)
Disease -
Reference -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 5
DNA change c.913G>A   (View in UCSC Genome Browser)
RNA change r.913g>a
Protein p.Ala305Thr
MAPP/PP2 Prior P 0.929
Prior P 0.900
IARC Classification Class 3: Uncertain
InSiGHT Classification Class 3: Uncertain
Tumour Char LR 0.100
Segregation LR 0.520
Odds for causality 0.052
Posterior P 0.3188
Reference Thompson et al., 2014, 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 5 c.913G>A r.913g>a p.Ala305Thr 0.929 0.900 Class 3: Uncertain Class 3: Uncertain 0.100 0.520 0.052 0.3188 Thompson et al., 2014, InSiGHT - DNA SEQ