NM_000352.6(ABCC8):c.-8G>T
|
rs200091822
|
0.00270
|
NM_000352.6(ABCC8):c.4545+13C>T
|
rs78338172
|
0.00212
|
NM_000352.6(ABCC8):c.1177-56G>A
|
rs183921963
|
0.00123
|
NM_000352.6(ABCC8):c.1874C>T (p.Ala625Val)
|
rs148709148
|
0.00093
|
NM_000352.6(ABCC8):c.3867+7G>A
|
rs372198547
|
0.00049
|
NM_000352.6(ABCC8):c.486C>T (p.Ile162=)
|
rs149872185
|
0.00038
|
NM_000352.6(ABCC8):c.3111C>T (p.Thr1037=)
|
rs201662945
|
0.00026
|
NM_000352.6(ABCC8):c.105G>A (p.Pro35=)
|
rs199925058
|
0.00024
|
NM_000352.6(ABCC8):c.3345G>A (p.Thr1115=)
|
rs186634115
|
0.00017
|
NM_000352.6(ABCC8):c.4412-14C>T
|
rs193922404
|
0.00016
|
NM_000352.6(ABCC8):c.823-8C>T
|
rs201000679
|
0.00014
|
NM_000352.6(ABCC8):c.4227C>T (p.Ile1409=)
|
rs146584228
|
0.00010
|
NM_000352.6(ABCC8):c.1486C>T (p.Leu496=)
|
rs150956385
|
0.00008
|
NM_000352.6(ABCC8):c.3858C>T (p.Tyr1286=)
|
rs377045545
|
0.00008
|
NM_000352.6(ABCC8):c.4116G>A (p.Gln1372=)
|
rs562715858
|
0.00008
|
NM_000352.6(ABCC8):c.3516C>T (p.Ile1172=)
|
rs142155036
|
0.00006
|
NM_000352.6(ABCC8):c.1536C>T (p.Tyr512=)
|
rs765090096
|
0.00004
|
NM_000352.6(ABCC8):c.2117-12C>A
|
rs193922398
|
0.00004
|
NM_000352.6(ABCC8):c.3618C>T (p.Thr1206=)
|
rs775134825
|
0.00004
|
NM_000352.6(ABCC8):c.4284C>T (p.Pro1428=)
|
rs986616476
|
0.00004
|
NM_000352.6(ABCC8):c.90G>A (p.Ala30=)
|
rs377209579
|
0.00004
|
NM_000352.6(ABCC8):c.3918C>G (p.Leu1306=)
|
rs372186045
|
0.00003
|
NM_000352.6(ABCC8):c.1716G>A (p.Ser572=)
|
rs750619309
|
0.00002
|
NM_000352.6(ABCC8):c.291-3C>T
|
rs764107333
|
0.00002
|
NM_000352.6(ABCC8):c.3557+20G>C
|
rs764779784
|
0.00002
|
NM_000352.6(ABCC8):c.4359C>T (p.Ala1453=)
|
rs769435360
|
0.00002
|
NM_000352.6(ABCC8):c.702C>T (p.Asn234=)
|
rs758289249
|
0.00002
|
NM_000352.6(ABCC8):c.3393C>T (p.Ile1131=)
|
rs776975807
|
0.00001
|
NM_000352.6(ABCC8):c.4119+10C>T
|
rs201955628
|
0.00001
|
NM_000352.6(ABCC8):c.4307+8C>G
|
rs1448472548
|
0.00001
|
NC_000011.10:g.17476972A>G
|
|
|
NM_000352.6(ABCC8):c.-10C>G
|
|
|
NM_000352.6(ABCC8):c.1104G>T (p.Leu368=)
|
|
|
NM_000352.6(ABCC8):c.1468-41G>A
|
|
|
NM_000352.6(ABCC8):c.1644G>A (p.Thr548=)
|
|
|
NM_000352.6(ABCC8):c.1672-26G>C
|
|
|
NM_000352.6(ABCC8):c.1672-4A>G
|
|
|
NM_000352.6(ABCC8):c.2041-12C>T
|
rs201419039
|
|
NM_000352.6(ABCC8):c.3435C>T (p.Ser1145=)
|
rs371089976
|
|
NM_000352.6(ABCC8):c.3650+4C>G
|
rs374315114
|
|
NM_000352.6(ABCC8):c.3834C>T (p.Gly1278=)
|
|
|
NM_000352.6(ABCC8):c.3867+7G>C
|
rs372198547
|
|