ClinVar Miner

List of variants in gene BCOR reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001123385.2(BCOR):c.223A>T (p.Thr75Ser) rs61744882 0.00055
NM_001123385.2(BCOR):c.2148C>T (p.Tyr716=) rs146426767 0.00017
NM_001123385.2(BCOR):c.3502+19G>A rs376361422 0.00016
NM_001123385.2(BCOR):c.2916C>T (p.Tyr972=) rs370067698 0.00014
NM_001123385.2(BCOR):c.2631C>T (p.Thr877=) rs780203470 0.00005
NM_001123385.2(BCOR):c.2910G>A (p.Ala970=) rs138137552 0.00005
NM_001123385.2(BCOR):c.3711G>A (p.Val1237=) rs753256966 0.00005
NM_001123385.2(BCOR):c.3951G>A (p.Pro1317=) rs972573105 0.00005
NM_001123385.2(BCOR):c.4152C>T (p.Tyr1384=) rs750973796 0.00005
NM_001123385.2(BCOR):c.1708G>A (p.Ala570Thr) rs748813798 0.00004
NM_001123385.2(BCOR):c.3052-14C>T rs373005644 0.00004
NM_001123385.2(BCOR):c.347C>T (p.Ser116Leu) rs775994643 0.00004
NM_001123385.2(BCOR):c.4599T>C (p.Pro1533=) rs189304389 0.00004
NM_001123385.2(BCOR):c.1668C>T (p.Asn556=) rs765752304 0.00003
NM_001123385.2(BCOR):c.2213C>T (p.Thr738Ile) rs767346654 0.00003
NM_001123385.2(BCOR):c.4053C>T (p.Thr1351=) rs781252900 0.00003
NM_001123385.2(BCOR):c.4902C>T (p.Ser1634=) rs747409134 0.00003
NM_001123385.2(BCOR):c.4944G>A (p.Pro1648=) rs1479323402 0.00003
NM_001123385.2(BCOR):c.1707C>T (p.Ser569=) rs1438078198 0.00001
NM_001123385.2(BCOR):c.2295C>T (p.Ser765=) rs1394435368 0.00001
NM_001123385.2(BCOR):c.2343C>T (p.Thr781=) rs754818592 0.00001
NM_001123385.2(BCOR):c.267C>G (p.Val89=) rs371808275 0.00001
NM_001123385.2(BCOR):c.2877A>G (p.Pro959=) rs763853464 0.00001
NM_001123385.2(BCOR):c.3349G>A (p.Ala1117Thr) rs374493655 0.00001
NM_001123385.2(BCOR):c.3847+17C>T rs749560832 0.00001
NM_001123385.2(BCOR):c.4080G>A (p.Lys1360=) rs1204263913 0.00001
NM_001123385.2(BCOR):c.4188A>G (p.Arg1396=) rs1340294679 0.00001
NM_001123385.2(BCOR):c.4485C>T (p.Asn1495=) rs754796420 0.00001
NM_001123385.2(BCOR):c.1680A>G (p.Ser560=) rs917209632
NM_001123385.2(BCOR):c.1902A>G (p.Pro634=) rs963000229
NM_001123385.2(BCOR):c.2091C>G (p.Ala697=)
NM_001123385.2(BCOR):c.2235G>A (p.Arg745=)
NM_001123385.2(BCOR):c.2265C>T (p.Tyr755=)
NM_001123385.2(BCOR):c.2409T>A (p.Leu803=) rs909983948
NM_001123385.2(BCOR):c.2460C>T (p.Asn820=)
NM_001123385.2(BCOR):c.2607T>C (p.Tyr869=)
NM_001123385.2(BCOR):c.2647G>A (p.Val883Ile) rs909942650
NM_001123385.2(BCOR):c.2650C>T (p.Leu884=) rs1442932290
NM_001123385.2(BCOR):c.2691G>A (p.Ser897=)
NM_001123385.2(BCOR):c.2694T>G (p.Thr898=) rs2147204732
NM_001123385.2(BCOR):c.285A>G (p.Gly95=) rs143135906
NM_001123385.2(BCOR):c.300A>G (p.Lys100=) rs775494265
NM_001123385.2(BCOR):c.3239-6C>T
NM_001123385.2(BCOR):c.3246T>C (p.Tyr1082=)
NM_001123385.2(BCOR):c.3305T>C (p.Val1102Ala) rs111622737
NM_001123385.2(BCOR):c.3417A>C (p.Ser1139=) rs1602130461
NM_001123385.2(BCOR):c.3450G>A (p.Glu1150=)
NM_001123385.2(BCOR):c.3693G>T (p.Arg1231=) rs2147054803
NM_001123385.2(BCOR):c.3747G>C (p.Gly1249=)
NM_001123385.2(BCOR):c.3834T>C (p.Ser1278=)
NM_001123385.2(BCOR):c.3848-20G>A
NM_001123385.2(BCOR):c.387C>A (p.Pro129=)
NM_001123385.2(BCOR):c.387C>G (p.Pro129=) rs769854762
NM_001123385.2(BCOR):c.3936A>G (p.Ala1312=)
NM_001123385.2(BCOR):c.3978A>G (p.Glu1326=)
NM_001123385.2(BCOR):c.4095C>G (p.Thr1365=)
NM_001123385.2(BCOR):c.4173+13C>A rs2147028349
NM_001123385.2(BCOR):c.4173+8T>C
NM_001123385.2(BCOR):c.4218C>T (p.Asp1406=) rs2147014917
NM_001123385.2(BCOR):c.4413C>G (p.Ala1471=) rs1602121380
NM_001123385.2(BCOR):c.4428+16C>T rs753776453
NM_001123385.2(BCOR):c.4533C>T (p.Asn1511=)
NM_001123385.2(BCOR):c.4578T>C (p.Ser1526=)
NM_001123385.2(BCOR):c.4595+9T>G
NM_001123385.2(BCOR):c.4596-10C>G
NM_001123385.2(BCOR):c.4644A>G (p.Leu1548=)
NM_001123385.2(BCOR):c.4741+8A>G
NM_001123385.2(BCOR):c.4976+17T>C
NM_001123385.2(BCOR):c.86+8C>G rs753791832
NM_001123385.2(BCOR):c.87-19G>A

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