ClinVar Miner

List of variants in gene BUB1B reported as uncertain significance for not provided

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001211.6(BUB1B):c.1001C>T (p.Pro334Leu) rs141953425 0.00063
NM_001211.6(BUB1B):c.1746A>C (p.Thr582=) rs373105304 0.00029
NM_001211.6(BUB1B):c.1412C>T (p.Thr471Met) rs117485407 0.00028
NM_001211.6(BUB1B):c.1227A>C (p.Glu409Asp) rs28989188 0.00027
NM_001211.6(BUB1B):c.1261C>T (p.Arg421Trp) rs201251790 0.00011
NM_001211.6(BUB1B):c.1478C>T (p.Thr493Ile) rs146795655 0.00011
NM_001211.6(BUB1B):c.1630C>T (p.Pro544Ser) rs138332995 0.00011
NM_001211.6(BUB1B):c.464A>G (p.Tyr155Cys) rs764923350 0.00006
NM_001211.6(BUB1B):c.1150A>G (p.Ser384Gly) rs202114756 0.00004
NM_001211.6(BUB1B):c.1382A>C (p.Gln461Pro) rs747886467 0.00004
NM_001211.6(BUB1B):c.581G>A (p.Arg194Gln) rs567916146 0.00002
NM_001211.6(BUB1B):c.1520A>G (p.Glu507Gly) rs750377734 0.00001
NM_001211.6(BUB1B):c.1825T>G (p.Cys609Gly) rs1217885669 0.00001
NM_001211.6(BUB1B):c.203T>G (p.Phe68Cys) rs2037144342 0.00001
NM_001211.6(BUB1B):c.104G>A (p.Gly35Glu) rs2140878494
NM_001211.6(BUB1B):c.1059-3653C>T rs185599777
NM_001211.6(BUB1B):c.1059-7del rs770579508
NM_001211.6(BUB1B):c.1168GAG[1] (p.Glu391del) rs778590557
NM_001211.6(BUB1B):c.1202AGA[1] (p.Lys402del) rs1566823816
NM_001211.6(BUB1B):c.1492_1493delinsTA (p.Val498Tyr) rs2037550680
NM_001211.6(BUB1B):c.151T>C (p.Cys51Arg) rs375885859
NM_001211.6(BUB1B):c.1567+2T>A rs1566825026
NM_001211.6(BUB1B):c.179G>A (p.Arg60Gln)
NM_001211.6(BUB1B):c.2129C>A (p.Thr710Asn)
NM_001211.6(BUB1B):c.2472C>G (p.Ser824Arg) rs1262972802
NM_001211.6(BUB1B):c.2549A>G (p.His850Arg)
NM_001211.6(BUB1B):c.704A>G (p.Lys235Arg) rs2140889871
NM_001211.6(BUB1B):c.727A>G (p.Ile243Val)

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