ClinVar Miner

List of variants in gene CYBB reported as benign

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Gene type:
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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_000397.4(CYBB):c.141+90C>A rs4422908 0.32673
NM_000397.4(CYBB):c.484-1068T>C rs12014060 0.21793
NM_000397.4(CYBB):c.804+118A>G rs5964125 0.16667
NM_000397.4(CYBB):c.483+78C>T rs6610669 0.16506
NM_000397.4(CYBB):c.142-338G>T rs4595265 0.11896
NM_000397.4(CYBB):c.1002G>A (p.Lys334=) rs2228117 0.05579
NM_000397.4(CYBB):c.483+204T>C rs17146242 0.05290
NM_000397.4(CYBB):c.141+48C>G rs7059081 0.05245
NM_000397.4(CYBB):c.674+261A>C rs35959988 0.04423
NM_000397.4(CYBB):c.675-316T>A rs34052166 0.04407
NM_000397.4(CYBB):c.484-258C>T rs35851882 0.04211
NM_000397.4(CYBB):c.338-304A>G rs34097325 0.03518
NM_000397.4(CYBB):c.1090G>C (p.Gly364Arg) rs141756032 0.00371
NM_000397.4(CYBB):c.654C>A (p.Gly218=) rs35080474 0.00303
NM_000397.4(CYBB):c.484-61A>G rs112709054 0.00189
NM_000397.4(CYBB):c.1551T>A (p.Asp517Glu) rs151344452 0.00144
NM_000397.4(CYBB):c.686G>A (p.Arg229His) rs139670417 0.00106
NM_000397.4(CYBB):c.46-7T>C rs182039020 0.00070
NM_000397.4(CYBB):c.338-13C>T rs193922447 0.00064
NM_000397.4(CYBB):c.1159G>A (p.Val387Ile) rs145620748 0.00043
NM_000397.4(CYBB):c.6G>C (p.Gly2=) rs372462475 0.00029
NM_000397.4(CYBB):c.805-17T>A rs182092761 0.00026
NM_000397.4(CYBB):c.1689C>T (p.Phe563=) rs567830215 0.00023
NM_000397.4(CYBB):c.1414G>A (p.Gly472Ser) rs13306300 0.00018
NM_000397.4(CYBB):c.855G>A (p.Leu285=) rs782293433 0.00018
NM_000397.4(CYBB):c.1685A>G (p.His562Arg) rs768055122 0.00013
NM_000397.4(CYBB):c.675-4C>T rs782223666 0.00013
NM_000397.4(CYBB):c.142-12C>T rs13306298 0.00009
NM_000397.4(CYBB):c.1158G>A (p.Ala386=) rs374511592 0.00007
NM_000397.4(CYBB):c.99T>C (p.Tyr33=) rs781937944 0.00007
NM_000397.4(CYBB):c.1203T>C (p.Tyr401=) rs782312337 0.00006
NM_000397.4(CYBB):c.1103C>T (p.Ala368Val) rs781935760 0.00005
NM_000397.4(CYBB):c.1701G>A (p.Lys567=) rs140774378 0.00005
NM_000397.4(CYBB):c.697G>A (p.Ala233Thr) rs374931542 0.00005
NM_000397.4(CYBB):c.1377A>G (p.Gln459=) rs782413959 0.00004
NM_000397.4(CYBB):c.1413C>T (p.Ala471=) rs782094378 0.00004
NM_000397.4(CYBB):c.171A>G (p.Ala57=) rs781824754 0.00004
NM_000397.4(CYBB):c.348C>T (p.Thr116=) rs782735382 0.00004
NM_000397.4(CYBB):c.1151+13T>C rs781868409 0.00003
NM_000397.4(CYBB):c.142-6T>C rs373947610 0.00003
NM_000397.4(CYBB):c.1300C>T (p.Leu434=) rs781891223 0.00002
NM_000397.4(CYBB):c.10T>A (p.Trp4Arg) rs782495755 0.00001
NM_000397.4(CYBB):c.1617T>C (p.Pro539=) rs187038548 0.00001
NM_000397.4(CYBB):c.549G>A (p.Thr183=) rs1556468340 0.00001
NM_000397.4(CYBB):c.663C>A (p.Ile221=) rs782727740 0.00001
NM_000397.4(CYBB):c.696C>T (p.Thr232=) rs782180981 0.00001
NM_000397.4(CYBB):c.1032C>G (p.Ser344=) rs782193225
NM_000397.4(CYBB):c.1071C>T (p.Ile357=)
NM_000397.4(CYBB):c.1090G>A (p.Gly364Arg) rs141756032
NM_000397.4(CYBB):c.1151+15C>A
NM_000397.4(CYBB):c.1152-16C>T
NM_000397.4(CYBB):c.1296C>T (p.Thr432=) rs782808570
NM_000397.4(CYBB):c.1314+16T>C
NM_000397.4(CYBB):c.1314+19C>T rs34834015
NM_000397.4(CYBB):c.1314+20G>A rs34290745
NM_000397.4(CYBB):c.1315-9del
NM_000397.4(CYBB):c.1497A>C (p.Lys499Asn) rs782201696
NM_000397.4(CYBB):c.1586+74_1586+76dup
NM_000397.4(CYBB):c.1681G>A (p.Val561Met) rs766756667
NM_000397.4(CYBB):c.216T>C (p.Cys72=) rs782202693
NM_000397.4(CYBB):c.483+13T>A
NM_000397.4(CYBB):c.484-60TG[19] rs57325016
NM_000397.4(CYBB):c.484-60TG[20] rs57325016
NM_000397.4(CYBB):c.484-60TG[21] rs57325016
NM_000397.4(CYBB):c.484-60TG[24] rs57325016
NM_000397.4(CYBB):c.484-60TG[25] rs57325016
NM_000397.4(CYBB):c.520T>C (p.Leu174=)
NM_000397.4(CYBB):c.60G>A (p.Gly20=)
NM_000397.4(CYBB):c.897+239TG[20] rs58302662
NM_000397.4(CYBB):c.897+239TG[22] rs58302662
NM_000397.4(CYBB):c.897+239TG[23] rs58302662
NM_000397.4(CYBB):c.897+239TG[24] rs58302662
NM_000397.4(CYBB):c.897+239TG[25] rs58302662

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