ClinVar Miner

Variants in gene VLDLR 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
181 12 1 12 8 0 0 19

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 uncertain significance likely benign benign
pathogenic 1 0 0 0
uncertain significance 0 0 7 4
likely benign 0 7 0 12
benign 0 4 12 0

All variants with conflicting interpretations #

Total variants: 19
Download table as spreadsheet
NM_003383.5(VLDLR):c.-42_-40GGC[5] rs71329437
NM_003383.5(VLDLR):c.-42_-40GGC[9] rs71329437
NM_003383.5(VLDLR):c.1162C>T (p.Leu388=) rs114172780
NM_003383.5(VLDLR):c.1342C>T (p.Arg448Ter) rs80338905
NM_003383.5(VLDLR):c.1343G>A (p.Arg448Gln) rs137946976
NM_003383.5(VLDLR):c.1458C>T (p.Ala486=) rs6143
NM_003383.5(VLDLR):c.175G>A (p.Val59Ile) rs6149
NM_003383.5(VLDLR):c.1809C>T (p.Asn603=) rs6147
NM_003383.5(VLDLR):c.2371G>A (p.Val791Ile) rs35334949
NM_003383.5(VLDLR):c.242A>G (p.Asn81Ser) rs140526335
NM_003383.5(VLDLR):c.24G>A (p.Ala8=) rs34336270
NM_003383.5(VLDLR):c.464G>C (p.Ser155Thr) rs34080096
NM_003383.5(VLDLR):c.468C>T (p.Pro156=) rs2242105
NM_003383.5(VLDLR):c.738C>T (p.Cys246=) rs116687040
NM_003383.5(VLDLR):c.75C>T (p.Thr25=) rs532555108
NM_003383.5(VLDLR):c.792C>T (p.Cys264=) rs141850403
NM_003383.5(VLDLR):c.902G>A (p.Arg301Gln) rs139671268
NM_003383.5(VLDLR):c.944-5T>C rs35782329
NM_003383.5(VLDLR):c.982A>G (p.Ser328Gly) rs116306908

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