ClinVar Miner

Variants in gene AARS1 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
413 73 2 15 12 0 4 28

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 1 3 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 3 1 0 11 5
likely benign 0 0 11 0 14
benign 0 0 5 14 2

All variants with conflicting interpretations #

Total variants: 28
Download table as spreadsheet
NM_001605.2(AARS1):c.1108A>G (p.Met370Val) rs199976742
NM_001605.2(AARS1):c.1275T>C (p.Thr425=) rs750552137
NM_001605.2(AARS1):c.1428G>C (p.Arg476=) rs80257731
NM_001605.2(AARS1):c.1481G>T (p.Ser494Ile) rs771059047
NM_001605.2(AARS1):c.1632C>T (p.Asp544=) rs149425243
NM_001605.2(AARS1):c.1672-4T>A rs187509039
NM_001605.2(AARS1):c.1685C>T (p.Thr562Ile) rs148355156
NM_001605.2(AARS1):c.1737C>T (p.Ile579=) rs144323646
NM_001605.2(AARS1):c.1993-4G>A rs528932248
NM_001605.2(AARS1):c.2166C>A (p.Phe722Leu) rs115882953
NM_001605.2(AARS1):c.2185C>T (p.Arg729Trp) rs138081804
NM_001605.2(AARS1):c.2333A>C (p.Glu778Ala) rs797044801
NM_001605.2(AARS1):c.2459A>G (p.Lys820Arg) rs147319762
NM_001605.2(AARS1):c.2521-3C>T rs200586605
NM_001605.2(AARS1):c.2580G>A (p.Leu860=) rs145581652
NM_001605.2(AARS1):c.2738G>A (p.Gly913Asp) rs369774476
NM_001605.2(AARS1):c.2791G>A (p.Gly931Ser) rs149377346
NM_001605.2(AARS1):c.2900A>T (p.Lys967Met) rs35744709
NM_001605.2(AARS1):c.518A>G (p.Asp173Gly) rs765398055
NM_001605.2(AARS1):c.561C>T (p.Cys187=) rs78523270
NM_001605.2(AARS1):c.600C>T (p.Ala200=) rs150080663
NM_001605.2(AARS1):c.64G>A (p.Glu22Lys) rs151091410
NM_001605.2(AARS1):c.741G>A (p.Leu247=) rs148075561
NM_001605.2(AARS1):c.904G>A (p.Ala302Thr) rs576221121
NM_001605.2(AARS1):c.95T>C (p.Ile32Thr) rs751721557
NM_001605.2(AARS1):c.976C>T (p.Arg326Trp) rs777601008
NM_001605.3(AARS1):c.259G>A rs763757370
NM_001605.3(AARS1):c.986G>A (p.Arg329His) rs267606621

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