ClinVar Miner

Variants in gene DNAJB6 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
97 49 0 5 10 0 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
uncertain significance 0 10 0
likely benign 10 0 5
benign 0 5 0

All variants with conflicting interpretations #

Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_058246.4(DNAJB6):c.276A>G (p.Thr92=) rs765815570
NM_058246.4(DNAJB6):c.279C>T (p.Phe93=) rs149278319
NM_058246.4(DNAJB6):c.429G>C (p.Ala143=) rs150709673
NM_058246.4(DNAJB6):c.48C>T (p.Pro16=) rs150583876
NM_058246.4(DNAJB6):c.564C>T (p.Phe188=) rs145897776
NM_058246.4(DNAJB6):c.602G>A (p.Arg201Lys) rs373070679
NM_058246.4(DNAJB6):c.706G>A (p.Asp236Asn) rs556999563
NM_058246.4(DNAJB6):c.815C>T (p.Ala272Val) rs978425267
NM_058246.4(DNAJB6):c.831T>G (p.Ser277=) rs369098407
NM_058246.4(DNAJB6):c.860G>A (p.Arg287Gln) rs368078459
NM_058246.4(DNAJB6):c.899-6C>T rs78337193
NM_058246.4(DNAJB6):c.948G>A (p.Ser316=) rs565527346
NM_058246.4(DNAJB6):c.961T>C (p.Ser321Pro) rs147168661
NM_058246.4(DNAJB6):c.962C>T (p.Ser321Leu) rs142974468
NM_058246.4(DNAJB6):c.974A>C (p.Asn325Thr)

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