ClinVar Miner

Variants in gene PALLD with conflicting interpretations

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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
196 9 0 3 12 1 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 risk factor
uncertain significance 0 4 9 0
likely benign 4 0 3 0
benign 9 3 0 1
risk factor 0 0 1 0

All variants with conflicting interpretations #

Total variants: 15
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NM_001166108.2(PALLD):c.1040C>T (p.Thr347Met) rs150711066
NM_001166108.2(PALLD):c.1273A>T (p.Thr425Ser) rs140454899
NM_001166108.2(PALLD):c.1289G>A (p.Arg430Gln) rs145571230
NM_001166108.2(PALLD):c.1394G>A (p.Arg465His) rs115372194
NM_001166108.2(PALLD):c.1849C>T (p.Arg617Cys) rs138283237
NM_001166108.2(PALLD):c.1965-12594T>G rs587780760
NM_001166108.2(PALLD):c.1965-12616C>T rs121908291
NM_001166108.2(PALLD):c.2084T>G (p.Leu695Arg) rs139375029
NM_001166108.2(PALLD):c.365C>T (p.Pro122Leu) rs116158771
NM_001166108.2(PALLD):c.413G>A (p.Arg138Gln) rs138665337
NM_001166108.2(PALLD):c.539C>T (p.Thr180Ile) rs146387060
NM_001166108.2(PALLD):c.556G>A (p.Ala186Thr)
NM_001166108.2(PALLD):c.731A>G (p.Gln244Arg) rs114946738
NM_001166108.2(PALLD):c.764G>A (p.Arg255His) rs146018183
NM_001166108.2(PALLD):c.909A>T (p.Arg303Ser) rs138897963

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