ClinVar Miner

Variants in gene VSX2 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 per condition Variants with at least 2 submissions on the same condition 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 conflict
431 4 0 5 15 0 2 21

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.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 2 2 0 0
likely pathogenic 2 0 1 0 0
uncertain significance 2 1 0 9 6
likely benign 0 0 9 0 3
benign 0 0 6 3 0

All variants with conflicting interpretations #

Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_182894.3(VSX2):c.831G>A (p.Leu277=) rs62006815 0.02860
NM_182894.3(VSX2):c.299C>A (p.Pro100Gln) rs35214083 0.00448
NM_182894.3(VSX2):c.522C>T (p.Asp174=) rs78509400 0.00273
NM_182894.3(VSX2):c.162C>A (p.Asp54Glu) rs61747367 0.00226
NM_182894.3(VSX2):c.699C>T (p.Pro233=) rs141712104 0.00082
NM_182894.3(VSX2):c.939T>A (p.Ala313=) rs372651860 0.00051
NM_182894.3(VSX2):c.171C>G (p.Ala57=) rs201395979 0.00038
NM_182894.3(VSX2):c.750G>A (p.Pro250=) rs192712847 0.00027
NM_182894.3(VSX2):c.579G>A (p.Gln193=) rs182972044 0.00024
NM_182894.3(VSX2):c.244G>A (p.Gly82Arg) rs375294678 0.00021
NM_182894.3(VSX2):c.249G>A (p.Gly83=) rs751526974 0.00016
NM_182894.3(VSX2):c.564G>A (p.Pro188=) rs201354547 0.00010
NM_182894.3(VSX2):c.504C>T (p.Asn168=) rs550984628 0.00005
NM_182894.3(VSX2):c.777G>A (p.Ser259=) rs371707151 0.00003
NM_182894.3(VSX2):c.679C>T (p.Arg227Trp) rs121912545 0.00002
NM_182894.3(VSX2):c.371-14C>T rs750778630 0.00001
NM_182894.3(VSX2):c.667G>A (p.Gly223Arg) rs755799430 0.00001
NM_182894.3(VSX2):c.599G>C (p.Arg200Pro) rs121912543
NM_182894.3(VSX2):c.760+11G>A rs777886580
NM_182894.3(VSX2):c.777G>T (p.Ser259=) rs371707151
NM_182894.3(VSX2):c.810C>G (p.Pro270=) rs759166720

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