ClinVar Miner

Variants in gene SIL1 with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission Variants with at least 2 submissions and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any kind of conflict
68 9 0 10 7 0 0 15

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

uncertain significance likely benign benign
uncertain significance 0 7 2
likely benign 7 0 10
benign 2 10 0

All variants with conflicting interpretations #

Total variants: 15
Download table as spreadsheet
NM_022464.4(SIL1):c.-6C>G rs11555154
NM_022464.4(SIL1):c.1029+6T>C rs57028146
NM_022464.4(SIL1):c.1167C>T (p.Pro389=) rs199890503
NM_022464.4(SIL1):c.153A>G (p.Thr51=) rs3088052
NM_022464.4(SIL1):c.239A>G (p.Gln80Arg) rs35581768
NM_022464.4(SIL1):c.274C>T (p.Arg92Trp) rs149242794
NM_022464.4(SIL1):c.368C>T (p.Thr123Ile) rs115800498
NM_022464.4(SIL1):c.394A>C (p.Lys132Gln) rs61745568
NM_022464.4(SIL1):c.454-6C>T rs58624842
NM_022464.4(SIL1):c.573G>A (p.Lys191=) rs148927511
NM_022464.4(SIL1):c.699T>C (p.Asn233=) rs140891877
NM_022464.4(SIL1):c.865-7C>T rs141796576
NM_022464.4(SIL1):c.900C>T (p.Phe300=) rs35080367
NM_022464.4(SIL1):c.933G>A (p.Gly311=) rs61744666
NM_022464.4(SIL1):c.984C>T (p.Leu328=) rs368666457

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