NM_000498.3(CYP11B2):c.*1340T>A
|
rs61763988
|
0.00124
|
NM_000498.3(CYP11B2):c.*789G>A
|
rs61763990
|
0.00095
|
NM_000498.3(CYP11B2):c.*993A>G
|
rs61763989
|
0.00012
|
NM_000498.3(CYP11B2):c.*504C>T
|
rs201487778
|
0.00010
|
NM_000498.3(CYP11B2):c.*205G>A
|
rs1296538192
|
0.00006
|
NM_000498.3(CYP11B2):c.*879G>A
|
rs375657023
|
0.00005
|
NM_000498.3(CYP11B2):c.845G>A (p.Arg282His)
|
rs769533897
|
0.00005
|
NM_000498.3(CYP11B2):c.*299G>A
|
rs528171695
|
0.00004
|
NM_000498.3(CYP11B2):c.979C>T (p.Leu327Phe)
|
rs769090647
|
0.00004
|
NM_000498.3(CYP11B2):c.*204C>G
|
rs773811282
|
0.00003
|
NM_000498.3(CYP11B2):c.280C>T (p.Pro94Ser)
|
rs1374018568
|
0.00003
|
NM_000498.3(CYP11B2):c.800-14T>C
|
rs563246146
|
0.00003
|
NM_000498.3(CYP11B2):c.*1047C>T
|
rs886062739
|
0.00002
|
NM_000498.3(CYP11B2):c.*746G>A
|
rs570202161
|
0.00002
|
NM_000498.3(CYP11B2):c.342G>A (p.Glu114=)
|
rs779683417
|
0.00002
|
NM_000498.3(CYP11B2):c.796T>G (p.Tyr266Asp)
|
rs779486718
|
0.00002
|
NM_000498.3(CYP11B2):c.*1277G>A
|
rs745532151
|
0.00001
|
NM_000498.3(CYP11B2):c.*431A>C
|
rs886062742
|
0.00001
|
NM_000498.3(CYP11B2):c.*613C>T
|
rs61757284
|
0.00001
|
NM_000498.3(CYP11B2):c.*759A>T
|
rs1035340238
|
0.00001
|
NM_000498.3(CYP11B2):c.1216T>G (p.Phe406Val)
|
rs1817560561
|
0.00001
|
NM_000498.3(CYP11B2):c.1343G>A (p.Arg448His)
|
rs1311444460
|
0.00001
|
NM_000498.3(CYP11B2):c.157C>T (p.Leu53=)
|
rs747248100
|
0.00001
|
NM_000498.3(CYP11B2):c.449C>T (p.Ser150Leu)
|
rs768685630
|
0.00001
|
NM_000498.3(CYP11B2):c.*25A>C
|
rs1817542488
|
|
NM_000498.3(CYP11B2):c.*298C>A
|
rs1380755213
|
|
NM_000498.3(CYP11B2):c.*591T>G
|
rs1817531890
|
|
NM_000498.3(CYP11B2):c.*743C>T
|
rs886062741
|
|
NM_000498.3(CYP11B2):c.*876C>A
|
rs1817525452
|
|
NM_000498.3(CYP11B2):c.*972C>G
|
rs886062740
|
|
NM_000498.3(CYP11B2):c.1136G>T (p.Gly379Val)
|
rs1409744694
|
|
NM_000498.3(CYP11B2):c.1201-9C>G
|
rs750931398
|
|
NM_000498.3(CYP11B2):c.1398+10C>T
|
rs1817553996
|
|
NM_000498.3(CYP11B2):c.1441A>T (p.Ile481Leu)
|
rs1817545728
|
|
NM_000498.3(CYP11B2):c.1454A>G (p.Tyr485Cys)
|
rs1817545422
|
|
NM_000498.3(CYP11B2):c.591A>G (p.Ile197Met)
|
rs886062744
|
|
NM_000498.3(CYP11B2):c.595+15G>T
|
rs886062743
|
|
NM_000498.3(CYP11B2):c.924T>C (p.Ser308=)
|
rs764640232
|
|