ClinVar Miner

Variants in gene ATP1A2 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
203 105 0 31 15 0 4 46

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 4 3 0 0
likely pathogenic 4 0 1 0 0
uncertain significance 3 1 0 12 7
likely benign 0 0 12 0 27
benign 0 0 7 27 0

All variants with conflicting interpretations #

Total variants: 46
Download table as spreadsheet
HGVS dbSNP
NM_000702.3(ATP1A2):c.-48C>G rs41265761
NM_000702.3(ATP1A2):c.1092G>A (p.Thr364=) rs55741021
NM_000702.3(ATP1A2):c.1119G>A (p.Ser373=) rs1063125
NM_000702.3(ATP1A2):c.1128G>A (p.Thr376=) rs374374188
NM_000702.3(ATP1A2):c.1203C>T (p.Thr401=) rs547954866
NM_000702.3(ATP1A2):c.1244C>T (p.Thr415Met) rs121918618
NM_000702.3(ATP1A2):c.1261C>T (p.Arg421Ter) rs1165052640
NM_000702.3(ATP1A2):c.129G>A (p.Lys43=) rs61734527
NM_000702.3(ATP1A2):c.1470C>T (p.Ile490=) rs111405592
NM_000702.3(ATP1A2):c.1474G>A (p.Glu492Lys) rs142348542
NM_000702.3(ATP1A2):c.152G>A (p.Arg51His) rs144106169
NM_000702.3(ATP1A2):c.1652-11C>G rs17846713
NM_000702.3(ATP1A2):c.1652-7C>A rs200102433
NM_000702.3(ATP1A2):c.1652-8C>T rs370023134
NM_000702.3(ATP1A2):c.1666A>T (p.Asn556Tyr) rs141467566
NM_000702.3(ATP1A2):c.1704C>T (p.Phe568=) rs17846714
NM_000702.3(ATP1A2):c.1761T>C (p.Ser587=) rs199621678
NM_000702.3(ATP1A2):c.1777C>T (p.Arg593Trp) rs886039530
NM_000702.3(ATP1A2):c.193C>T (p.Arg65Trp) rs121918619
NM_000702.3(ATP1A2):c.194G>T (p.Arg65Leu) rs187733403
NM_000702.3(ATP1A2):c.1980C>T (p.Cys660=) rs61734529
NM_000702.3(ATP1A2):c.2066G>A (p.Arg689Gln) rs28933401
NM_000702.3(ATP1A2):c.2130C>T (p.Ala710=) rs374749325
NM_000702.3(ATP1A2):c.2143G>A (p.Gly715Arg) rs1553245771
NM_000702.3(ATP1A2):c.2259C>T (p.Ala753=) rs17846715
NM_000702.3(ATP1A2):c.2438T>A (p.Met813Lys) rs796052277
NM_000702.3(ATP1A2):c.246C>G (p.Pro82=) rs537472446
NM_000702.3(ATP1A2):c.2514G>A (p.Thr838=) rs140646289
NM_000702.3(ATP1A2):c.2563+4C>T rs3747626
NM_000702.3(ATP1A2):c.2564-8A>G rs554846350
NM_000702.3(ATP1A2):c.25T>A (p.Tyr9Asn) rs55858252
NM_000702.3(ATP1A2):c.2751G>A (p.Thr917=) rs146839867
NM_000702.3(ATP1A2):c.2877G>A (p.Thr959=) rs200127278
NM_000702.3(ATP1A2):c.2936C>T (p.Pro979Leu) rs121918615
NM_000702.3(ATP1A2):c.2943-15C>T rs111510835
NM_000702.3(ATP1A2):c.2961C>T (p.Cys987=) rs74123254
NM_000702.3(ATP1A2):c.2967C>T (p.Phe989=) rs138826759
NM_000702.3(ATP1A2):c.2973C>T (p.Tyr991=) rs149286529
NM_000702.3(ATP1A2):c.3034+14C>T rs41288127
NM_000702.3(ATP1A2):c.3034+6C>A rs574788908
NM_000702.3(ATP1A2):c.339C>T (p.Tyr113=) rs148929192
NM_000702.3(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766
NM_000702.3(ATP1A2):c.471T>C (p.Asp157=) rs553035942
NM_000702.3(ATP1A2):c.627T>C (p.Cys209=) rs139229302
NM_000702.3(ATP1A2):c.836G>A (p.Arg279Gln) rs373178892
NM_000702.3(ATP1A2):c.8G>A (p.Arg3His) rs781687346

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