ClinVar Miner

Variants in gene NIN 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
98 5 0 11 4 0 1 16

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 0 1 0 0
uncertain significance 1 0 2 2
likely benign 0 2 0 11
benign 0 2 11 0

All variants with conflicting interpretations #

Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_020921.3(NIN):c.1728G>A (p.Pro576=) rs61755036
NM_020921.3(NIN):c.264A>T (p.Pro88=) rs61755037
NM_020921.3(NIN):c.2665G>C (p.Val889Leu) rs78251482
NM_020921.3(NIN):c.2987C>T (p.Ala996Val) rs41313507
NM_020921.3(NIN):c.3454G>T (p.Val1152Phe) rs61742284
NM_020921.3(NIN):c.447G>A (p.Thr149=) rs547438612
NM_020921.3(NIN):c.4674G>A (p.Thr1558=) rs45578537
NM_020921.3(NIN):c.4866A>C (p.Glu1622Asp) rs77959782
NM_020921.3(NIN):c.4937G>A (p.Arg1646His) rs149669464
NM_020921.3(NIN):c.5075G>A (p.Cys1692Tyr) rs75544578
NM_020921.3(NIN):c.5126A>G (p.Asn1709Ser) rs387907308
NM_020921.3(NIN):c.5188T>C (p.Leu1730=) rs61741547
NM_020921.3(NIN):c.5903C>T (p.Thr1968Met) rs61744312
NM_020921.3(NIN):c.600T>C (p.Gly200=) rs61740039
NM_020921.3(NIN):c.6068A>G (p.Asn2023Ser) rs61747997
NM_020921.3(NIN):c.612G>A (p.Arg204=) rs150057118

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