ClinVar Miner

List of variants in gene SBF2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 45
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HGVS dbSNP
NC_000011.10:g.9832210_9832211del
NM_030962.3(SBF2):c.*20C>G rs1057523279
NM_030962.3(SBF2):c.1054-11T>C rs1554976748
NM_030962.3(SBF2):c.1296+296A>G
NM_030962.3(SBF2):c.129G>A (p.Gln43=) rs761285505
NM_030962.3(SBF2):c.1396-295T>C
NM_030962.3(SBF2):c.141+258C>T
NM_030962.3(SBF2):c.142-11A>G rs539146891
NM_030962.3(SBF2):c.1491T>C (p.Asn497=) rs767806871
NM_030962.3(SBF2):c.1509A>G (p.Glu503=) rs143773975
NM_030962.3(SBF2):c.1812C>T (p.Asp604=) rs765658939
NM_030962.3(SBF2):c.1860+10A>G rs778305149
NM_030962.3(SBF2):c.21C>T (p.Tyr7=) rs1555111778
NM_030962.3(SBF2):c.280-193G>A
NM_030962.3(SBF2):c.3652+6C>T rs1057524041
NM_030962.3(SBF2):c.3979-4G>T rs375742620
NM_030962.3(SBF2):c.402+15G>A rs780717348
NM_030962.3(SBF2):c.403-15T>G rs887143579
NM_030962.3(SBF2):c.4068G>A (p.Leu1356=) rs1429589073
NM_030962.3(SBF2):c.4095C>T (p.Ile1365=) rs142904756
NM_030962.3(SBF2):c.4128G>A (p.Ala1376=) rs191964053
NM_030962.3(SBF2):c.4444-18T>G rs143439179
NM_030962.3(SBF2):c.4509C>T (p.His1503=) rs138816399
NM_030962.3(SBF2):c.4693A>G (p.Ile1565Val) rs115345208
NM_030962.3(SBF2):c.4698+15C>G rs1554901068
NM_030962.3(SBF2):c.492C>G (p.Val164=) rs559769224
NM_030962.3(SBF2):c.5034T>C (p.Asp1678=) rs771306445
NM_030962.3(SBF2):c.5037+12A>G rs372500490
NM_030962.3(SBF2):c.5037C>T (p.Arg1679=) rs200784979
NM_030962.3(SBF2):c.5055G>A (p.Ser1685=) rs375798441
NM_030962.3(SBF2):c.513+18A>T rs201201683
NM_030962.3(SBF2):c.513+297G>A
NM_030962.3(SBF2):c.514-12C>T rs770141264
NM_030962.3(SBF2):c.5231+14C>T rs371184526
NM_030962.3(SBF2):c.5231+19C>T rs1250788397
NM_030962.3(SBF2):c.5310A>G (p.Thr1770=) rs1057521006
NM_030962.3(SBF2):c.5319+52C>T
NM_030962.3(SBF2):c.5319+7C>T rs1057521682
NM_030962.3(SBF2):c.5451+10_5451+13dup rs1064795190
NM_030962.3(SBF2):c.620-9T>C rs199676895
NM_030962.3(SBF2):c.753-16T>C rs7128234
NM_030962.3(SBF2):c.807A>T (p.Pro269=) rs1057521879
NM_030962.3(SBF2):c.862-99A>C
NM_030962.3(SBF2):c.862-9C>A rs1554979581
NM_030962.3(SBF2):c.993G>A (p.Leu331=) rs766193938

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