ClinVar Miner

Variants in gene ARID1B 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
350 44 0 19 14 0 1 33

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

All variants with conflicting interpretations #

Total variants: 33
Download table as spreadsheet
HGVS dbSNP
NM_001346813.1(ARID1B):c.1049_1051dup (p.Ala350_Gly351insAla) rs797045267
NM_001346813.1(ARID1B):c.360_362dup (p.Gln131_His132insGln) rs587779743
NM_001346813.1(ARID1B):c.381_386dup (p.Gln131_His132insGlnGln) rs587779744
NM_001346813.1(ARID1B):c.942_944dup (p.Gly319_Ser320insGly) rs587779747
NM_020732.3(ARID1B):c.1029_1043del15 (p.Ala346_Ala350del) rs775733700
NM_020732.3(ARID1B):c.1041_1043dup (p.Ala350_Gly351insAla)
NM_020732.3(ARID1B):c.1069_1071delGGC (p.Gly357del) rs797045268
NM_020732.3(ARID1B):c.1069_1071dup (p.Gly357_Tyr358insGly) rs797045268
NM_020732.3(ARID1B):c.121_123delTCC (p.Ser41del) rs770512547
NM_020732.3(ARID1B):c.1678A>G (p.Ile560Val) rs17318151
NM_020732.3(ARID1B):c.1762G>T (p.Glu588Ter) rs201653711
NM_020732.3(ARID1B):c.1960C>T (p.Gln654Ter) rs1554270809
NM_020732.3(ARID1B):c.1977C>T (p.Pro659=) rs146240413
NM_020732.3(ARID1B):c.2895C>T (p.Pro965=) rs144894118
NM_020732.3(ARID1B):c.2896G>A (p.Gly966Ser) rs34786733
NM_020732.3(ARID1B):c.2985G>A (p.Pro995=) rs537901478
NM_020732.3(ARID1B):c.3025+6C>T rs148976215
NM_020732.3(ARID1B):c.357_362dupGCAGCA (p.Gln131_His132insGlnGln) rs587779743
NM_020732.3(ARID1B):c.384_386delGCA (p.Gln131del) rs587779744
NM_020732.3(ARID1B):c.384_386dupGCA (p.Gln131_His132insGln) rs587779744
NM_020732.3(ARID1B):c.3946G>A (p.Gly1316Arg) rs199674889
NM_020732.3(ARID1B):c.4110G>A (p.Pro1370=) rs797045277
NM_020732.3(ARID1B):c.4495A>T (p.Met1499Leu) rs34870395
NM_020732.3(ARID1B):c.4658C>T (p.Ala1553Val) rs762698567
NM_020732.3(ARID1B):c.5015A>G (p.Asn1672Ser) rs140177120
NM_020732.3(ARID1B):c.5338C>T (p.Gln1780Ter) rs750447037
NM_020732.3(ARID1B):c.5394_5397del (p.Phe1798Leufs) rs1554237269
NM_020732.3(ARID1B):c.5802C>T (p.Ile1934=) rs142499766
NM_020732.3(ARID1B):c.6594G>A (p.Ala2198=) rs754242891
NM_020732.3(ARID1B):c.6654C>T (p.His2218=) rs183572405
NM_020732.3(ARID1B):c.679_680delGTinsCC (p.Val227Pro) rs1554247605
NM_020732.3(ARID1B):c.942C>A (p.Gly314=) rs184815562
NM_020732.3(ARID1B):c.980_985delGAGGAG (p.Gly327_Gly328del) rs747790383

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