ClinVar Miner

Variants in gene combination PRSS1, TRB with conflicting interpretations

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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
109 10 6 9 7 0 3 21

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 6 1 2 1 1
likely pathogenic 1 0 0 0 0
uncertain significance 2 0 0 5 3
likely benign 1 0 5 0 8
benign 1 0 3 8 0

All variants with conflicting interpretations #

Total variants: 21
Download table as spreadsheet
HGVS dbSNP
NM_002769.4(PRSS1):c.40+40delC rs748794481
NM_002769.5(PRSS1):c.121C>T (p.Leu41=) rs369646357
NM_002769.5(PRSS1):c.200+1G>A rs143909348
NM_002769.5(PRSS1):c.235G>A (p.Glu79Lys) rs111033564
NM_002769.5(PRSS1):c.279C>T (p.Ile93=) rs139664510
NM_002769.5(PRSS1):c.346C>T (p.Arg116Cys) rs387906698
NM_002769.5(PRSS1):c.360C>T (p.Asn120=) rs606231348
NM_002769.5(PRSS1):c.364C>T (p.Arg122Cys) rs111033568
NM_002769.5(PRSS1):c.365G>A (p.Arg122His) rs111033565
NM_002769.5(PRSS1):c.390C>T (p.Thr130=) rs561097415
NM_002769.5(PRSS1):c.410C>T (p.Thr137Met) rs117497341
NM_002769.5(PRSS1):c.417C>T (p.Cys139=) rs141847266
NM_002769.5(PRSS1):c.453C>T (p.Gly151=) rs147765409
NM_002769.5(PRSS1):c.47C>T (p.Ala16Val) rs202003805
NM_002769.5(PRSS1):c.486T>C (p.Asp162=) rs6666
NM_002769.5(PRSS1):c.567T>C (p.Leu189=) rs377124851
NM_002769.5(PRSS1):c.623G>C (p.Gly208Ala) rs189270875
NM_002769.5(PRSS1):c.68A>G (p.Lys23Arg) rs111033567
NM_002769.5(PRSS1):c.738T>C (p.Asn246=) rs6667
NM_002769.5(PRSS1):c.86A>T (p.Asn29Ile) rs111033566
NM_002769.5(PRSS1):c.93G>A (p.Glu31=) rs745623963

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