ClinVar Miner

Variants in gene BAG3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 31
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HGVS dbSNP gnomAD frequency
NM_004281.4(BAG3):c.451T>C (p.Cys151Arg) rs2234962 0.14532
NM_004281.4(BAG3):c.231G>A (p.Pro77=) rs143752613 0.00441
NM_004281.4(BAG3):c.606G>T (p.Pro202=) rs74157690 0.00341
NM_004281.4(BAG3):c.1138C>T (p.Pro380Ser) rs144692954 0.00327
NM_004281.4(BAG3):c.181-9T>A rs139232658 0.00317
NM_004281.4(BAG3):c.463G>A (p.Ala155Thr) rs61756328 0.00239
NM_004281.4(BAG3):c.-17G>A rs200388926 0.00218
NM_004281.4(BAG3):c.25A>G (p.Met9Val) rs137965903 0.00175
NM_004281.4(BAG3):c.1587C>T (p.Ala529=) rs149358702 0.00144
NM_004281.4(BAG3):c.549C>G (p.Ser183=) rs112929734 0.00141
NM_004281.4(BAG3):c.1436C>T (p.Ala479Val) rs34656239 0.00097
NM_004281.4(BAG3):c.1503C>A (p.Val501=) rs147277075 0.00089
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe) rs145393807 0.00085
NM_004281.4(BAG3):c.870C>G (p.Pro290=) rs140737221 0.00055
NM_004281.4(BAG3):c.855G>A (p.Thr285=) rs147259596 0.00048
NM_004281.4(BAG3):c.888C>T (p.His296=) rs139399890 0.00040
NM_004281.4(BAG3):c.821C>T (p.Ser274Leu) rs143919208 0.00038
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp) rs117671123 0.00036
NM_004281.4(BAG3):c.230C>T (p.Pro77Leu) rs141355480 0.00033
NM_004281.4(BAG3):c.771C>T (p.Pro257=) rs200212999 0.00028
NM_004281.4(BAG3):c.898G>A (p.Asp300Asn) rs78439745 0.00026
NM_004281.4(BAG3):c.1240G>A (p.Glu414Lys) rs117749531 0.00024
NM_004281.4(BAG3):c.96G>T (p.Pro32=) rs372083121 0.00017
NM_004281.4(BAG3):c.1029C>A (p.Arg343=) rs117972572 0.00013
NM_004281.4(BAG3):c.693G>A (p.Thr231=) rs144034433 0.00006
NM_004281.4(BAG3):c.627G>A (p.Pro209=) rs188555685 0.00004
NM_004281.4(BAG3):c.483G>A (p.Gln161=) rs758279156 0.00003
NM_004281.4(BAG3):c.897C>T (p.Val299=) rs763915884 0.00002
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.4(BAG3):c.468GGC[4] (p.Ala160dup) rs139438727
NM_004281.4(BAG3):c.612G>A (p.Gly204=) rs2134065088

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