ClinVar Miner

Variants in gene BAG3 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
157 79 1 25 19 0 3 44

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 1 5 2 0 0
likely pathogenic 5 0 1 0 0
uncertain significance 2 1 0 17 6
likely benign 0 0 17 0 20
benign 0 0 6 20 0

All variants with conflicting interpretations #

Total variants: 44
Download table as spreadsheet
HGVS dbSNP
NM_004281.3(BAG3):c.-17G>A rs200388926
NM_004281.3(BAG3):c.1138C>T (p.Pro380Ser) rs144692954
NM_004281.3(BAG3):c.1240G>A (p.Glu414Lys) rs117749531
NM_004281.3(BAG3):c.1363G>A (p.Glu455Lys) rs397516881
NM_004281.3(BAG3):c.1385T>C (p.Leu462Pro) rs397514507
NM_004281.3(BAG3):c.1423G>A (p.Asp475Asn) rs138832242
NM_004281.3(BAG3):c.1436C>T (p.Ala479Val) rs34656239
NM_004281.3(BAG3):c.1503C>A (p.Val501=) rs147277075
NM_004281.3(BAG3):c.1587C>T (p.Ala529=) rs149358702
NM_004281.3(BAG3):c.1588G>A (p.Val530Met) rs144678100
NM_004281.3(BAG3):c.1630G>C (p.Asp544His) rs786205466
NM_004281.3(BAG3):c.181-15C>T rs397516882
NM_004281.3(BAG3):c.211C>T (p.Arg71Trp) rs387906874
NM_004281.3(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.3(BAG3):c.212G>T (p.Arg71Leu) rs35434411
NM_004281.3(BAG3):c.230C>T (p.Pro77Leu) rs141355480
NM_004281.3(BAG3):c.231G>A (p.Pro77=) rs143752613
NM_004281.3(BAG3):c.249C>A (p.His83Gln) rs151331972
NM_004281.3(BAG3):c.25A>G (p.Met9Val) rs137965903
NM_004281.3(BAG3):c.280A>T (p.Ile94Phe) rs145393807
NM_004281.3(BAG3):c.367C>T (p.Arg123Ter) rs387906875
NM_004281.3(BAG3):c.400T>A (p.Ser134Thr) rs375257731
NM_004281.3(BAG3):c.415C>T (p.Arg139Trp) rs556465096
NM_004281.3(BAG3):c.460G>A (p.Val154Met) rs376198104
NM_004281.3(BAG3):c.463G>A (p.Ala155Thr) rs61756328
NM_004281.3(BAG3):c.465A>G (p.Ala155=) rs775151738
NM_004281.3(BAG3):c.467C>G (p.Ala156Gly) rs572038196
NM_004281.3(BAG3):c.474_476dupGGC (p.Ala160_Gln161insAla) rs139438727
NM_004281.3(BAG3):c.498C>T (p.His166=) rs111682654
NM_004281.3(BAG3):c.549C>G (p.Ser183=) rs112929734
NM_004281.3(BAG3):c.606G>T (p.Pro202=) rs74157690
NM_004281.3(BAG3):c.626C>T (p.Pro209Leu) rs121918312
NM_004281.3(BAG3):c.627G>A (p.Pro209=) rs188555685
NM_004281.3(BAG3):c.652C>T (p.Arg218Trp) rs397514506
NM_004281.3(BAG3):c.653G>A (p.Arg218Gln) rs201638005
NM_004281.3(BAG3):c.699C>A (p.Tyr233Ter) rs876661342
NM_004281.3(BAG3):c.730C>T (p.Gln244Ter) rs876657634
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp) rs117671123
NM_004281.3(BAG3):c.821C>T (p.Ser274Leu) rs143919208
NM_004281.3(BAG3):c.855G>A (p.Thr285=) rs147259596
NM_004281.3(BAG3):c.870C>G (p.Pro290=) rs140737221
NM_004281.3(BAG3):c.888C>T (p.His296=) rs139399890
NM_004281.3(BAG3):c.898G>A (p.Asp300Asn) rs78439745
NM_004281.3(BAG3):c.96G>T (p.Pro32=) rs372083121

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