NM_000626.4(CD79B):c.67+10C>A
|
rs112931479
|
0.00106
|
NM_000626.4(CD79B):c.431-4G>A
|
rs201051431
|
0.00059
|
NM_000626.4(CD79B):c.549+16G>A
|
rs200501913
|
0.00037
|
NM_000626.4(CD79B):c.468G>A (p.Thr156=)
|
rs114813228
|
0.00019
|
NM_000626.4(CD79B):c.592-6C>G
|
rs372665115
|
0.00019
|
NM_000626.4(CD79B):c.118+19C>T
|
rs200473170
|
0.00016
|
NM_000626.4(CD79B):c.48G>A (p.Ala16=)
|
rs758062682
|
0.00015
|
NM_000626.4(CD79B):c.645A>G (p.Thr215=)
|
rs375009834
|
0.00014
|
NM_000626.4(CD79B):c.303C>T (p.Asn101=)
|
rs115494685
|
0.00012
|
NM_000626.4(CD79B):c.549+14G>A
|
rs371496789
|
0.00010
|
NM_000626.4(CD79B):c.498G>A (p.Thr166=)
|
rs141754572
|
0.00009
|
NM_000626.4(CD79B):c.68-9A>G
|
rs374896622
|
0.00009
|
NM_000626.4(CD79B):c.648G>A (p.Gly216=)
|
rs138535790
|
0.00008
|
NM_000626.4(CD79B):c.118+13G>A
|
rs543290517
|
0.00004
|
NM_000626.4(CD79B):c.431-3C>T
|
rs764645960
|
0.00004
|
NM_000626.4(CD79B):c.255T>C (p.Asn85=)
|
rs762226211
|
0.00002
|
NM_000626.4(CD79B):c.261G>A (p.Gln87=)
|
rs191761650
|
0.00002
|
NM_000626.4(CD79B):c.408C>T (p.Cys136=)
|
rs749042260
|
0.00002
|
NM_000626.4(CD79B):c.430+10A>C
|
rs758503702
|
0.00002
|
NM_000626.4(CD79B):c.636G>A (p.Thr212=)
|
rs534051167
|
0.00002
|
NM_000626.4(CD79B):c.15G>A (p.Ala5=)
|
rs199930415
|
0.00001
|
NM_000626.4(CD79B):c.213C>T (p.Ser71=)
|
rs756340178
|
0.00001
|
NM_000626.4(CD79B):c.351T>C (p.Asn117=)
|
rs760407063
|
0.00001
|
NM_000626.4(CD79B):c.390G>A (p.Ser130=)
|
rs1374878972
|
0.00001
|
NM_000626.4(CD79B):c.405C>T (p.Gly135=)
|
rs11555058
|
0.00001
|
NM_000626.4(CD79B):c.431-19C>T
|
rs1908012295
|
0.00001
|
NM_000626.4(CD79B):c.431-5C>T
|
rs554783299
|
0.00001
|
NM_000626.4(CD79B):c.522C>T (p.Ile174=)
|
rs115099162
|
0.00001
|
NM_000626.4(CD79B):c.549+11G>A
|
rs772302337
|
0.00001
|
NM_000626.4(CD79B):c.67+18A>G
|
rs773415844
|
0.00001
|
NM_000626.4(CD79B):c.100C>A (p.Arg34=)
|
rs1350196178
|
|
NM_000626.4(CD79B):c.102G>A (p.Arg34=)
|
rs549278202
|
|
NM_000626.4(CD79B):c.118+15C>T
|
|
|
NM_000626.4(CD79B):c.119-7C>T
|
rs2144758434
|
|
NM_000626.4(CD79B):c.120T>A (p.Gly40=)
|
rs1598400558
|
|
NM_000626.4(CD79B):c.132G>A (p.Ser44=)
|
|
|
NM_000626.4(CD79B):c.144G>A (p.Gln48=)
|
|
|
NM_000626.4(CD79B):c.162C>T (p.Ala54=)
|
|
|
NM_000626.4(CD79B):c.165G>A (p.Arg55=)
|
rs747800058
|
|
NM_000626.4(CD79B):c.213C>G (p.Ser71=)
|
rs756340178
|
|
NM_000626.4(CD79B):c.225C>T (p.Ser75=)
|
|
|
NM_000626.4(CD79B):c.24T>C (p.Pro8=)
|
|
|
NM_000626.4(CD79B):c.279G>A (p.Lys93=)
|
|
|
NM_000626.4(CD79B):c.282C>T (p.Gly94=)
|
rs2144757951
|
|
NM_000626.4(CD79B):c.294G>A (p.Glu98=)
|
|
|
NM_000626.4(CD79B):c.354C>T (p.Gly118=)
|
rs2144757727
|
|
NM_000626.4(CD79B):c.363C>T (p.Phe121=)
|
|
|
NM_000626.4(CD79B):c.372G>A (p.Gln124=)
|
rs745434907
|
|
NM_000626.4(CD79B):c.381C>T (p.Asn127=)
|
rs1555598971
|
|
NM_000626.4(CD79B):c.387C>T (p.Thr129=)
|
|
|
NM_000626.4(CD79B):c.430+8C>A
|
rs780195935
|
|
NM_000626.4(CD79B):c.431-13C>T
|
|
|
NM_000626.4(CD79B):c.431-15C>A
|
|
|
NM_000626.4(CD79B):c.431-18C>G
|
|
|
NM_000626.4(CD79B):c.431-18C>T
|
|
|
NM_000626.4(CD79B):c.431-20C>A
|
|
|
NM_000626.4(CD79B):c.431-20C>T
|
|
|
NM_000626.4(CD79B):c.462G>A (p.Arg154=)
|
|
|
NM_000626.4(CD79B):c.480T>A (p.Gly160=)
|
|
|
NM_000626.4(CD79B):c.48G>C (p.Ala16=)
|
rs758062682
|
|
NM_000626.4(CD79B):c.501G>A (p.Leu167=)
|
|
|
NM_000626.4(CD79B):c.534C>T (p.Phe178=)
|
|
|
NM_000626.4(CD79B):c.549+11G>T
|
rs772302337
|
|
NM_000626.4(CD79B):c.549+13C>T
|
|
|
NM_000626.4(CD79B):c.549+17G>T
|
|
|
NM_000626.4(CD79B):c.549+20A>G
|
|
|
NM_000626.4(CD79B):c.549+9G>A
|
|
|
NM_000626.4(CD79B):c.549+9G>C
|
|
|
NM_000626.4(CD79B):c.550-19C>A
|
|
|
NM_000626.4(CD79B):c.550-6C>T
|
rs748612433
|
|
NM_000626.4(CD79B):c.567C>T (p.Gly189=)
|
rs143511067
|
|
NM_000626.4(CD79B):c.585C>G (p.Thr195=)
|
rs1907978089
|
|
NM_000626.4(CD79B):c.591+13G>A
|
rs371044426
|
|
NM_000626.4(CD79B):c.591+16G>A
|
|
|
NM_000626.4(CD79B):c.621T>C (p.Tyr207=)
|
|
|
NM_000626.4(CD79B):c.669T>C (p.Gly223=)
|
|
|
NM_000626.4(CD79B):c.67+14G>A
|
|
|
NM_000626.4(CD79B):c.67+16C>T
|
|
|
NM_000626.4(CD79B):c.67+19G>A
|
|
|
NM_000626.4(CD79B):c.67+9C>A
|
rs2144762223
|
|
NM_000626.4(CD79B):c.672G>A (p.Glu224=)
|
|
|
NM_000626.4(CD79B):c.678A>C (p.Pro226=)
|
rs2144755338
|
|
NM_000626.4(CD79B):c.68-5A>G
|
rs943927329
|
|
NM_000626.4(CD79B):c.68-7C>T
|
|
|
NM_000626.4(CD79B):c.75A>C (p.Pro25=)
|
rs2144760436
|
|
NM_000626.4(CD79B):c.93G>A (p.Ser31=)
|
|
|