ClinVar Miner

List of variants in gene ABCC8 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 127
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HGVS dbSNP
NM_000352.6(ABCC8):c.1002C>T (p.Phe334=) rs763978514
NM_000352.6(ABCC8):c.1012-6C>T rs764178736
NM_000352.6(ABCC8):c.105G>A (p.Pro35=) rs199925058
NM_000352.6(ABCC8):c.1071C>G (p.Val357=) rs747552453
NM_000352.6(ABCC8):c.108C>T (p.His36=) rs757935183
NM_000352.6(ABCC8):c.1095C>T (p.Ala365=) rs1256418853
NM_000352.6(ABCC8):c.1296C>T (p.Phe432=) rs1591845922
NM_000352.6(ABCC8):c.1368C>T (p.Leu456=) rs775001123
NM_000352.6(ABCC8):c.1416T>C (p.Pro472=) rs1391155490
NM_000352.6(ABCC8):c.1428C>T (p.Phe476=) rs867541142
NM_000352.6(ABCC8):c.1467+9C>T rs774224706
NM_000352.6(ABCC8):c.1486C>T (p.Leu496=) rs150956385
NM_000352.6(ABCC8):c.1512C>T (p.Arg504=) rs148811815
NM_000352.6(ABCC8):c.1536C>T (p.Tyr512=) rs765090096
NM_000352.6(ABCC8):c.1548C>T (p.Asn516=) rs776590557
NM_000352.6(ABCC8):c.1617T>C (p.Tyr539=) rs1591832463
NM_000352.6(ABCC8):c.1644G>T (p.Thr548=) rs565996783
NM_000352.6(ABCC8):c.165C>T (p.Ser55=) rs1591928903
NM_000352.6(ABCC8):c.1668C>T (p.Leu556=) rs1287759139
NM_000352.6(ABCC8):c.1704G>A (p.Glu568=) rs745652559
NM_000352.6(ABCC8):c.1716G>T (p.Ser572=) rs750619309
NM_000352.6(ABCC8):c.1767G>T (p.Pro589=) rs550788491
NM_000352.6(ABCC8):c.1818-6G>A rs368708177
NM_000352.6(ABCC8):c.1818-7C>T rs17846731
NM_000352.6(ABCC8):c.1858C>T (p.Arg620Cys) rs58241708
NM_000352.6(ABCC8):c.1874C>T (p.Ala625Val) rs148709148
NM_000352.6(ABCC8):c.1920G>A (p.Ala640=) rs146156937
NM_000352.6(ABCC8):c.1923+10C>T rs775087598
NM_000352.6(ABCC8):c.1938G>A (p.Val646=) rs1591797830
NM_000352.6(ABCC8):c.1980C>T (p.Thr660=) rs766374930
NM_000352.6(ABCC8):c.1998G>C (p.Leu666=) rs1191652273
NM_000352.6(ABCC8):c.2022T>C (p.Ala674=) rs371724951
NM_000352.6(ABCC8):c.2060C>T (p.Thr687Met) rs150316347
NM_000352.6(ABCC8):c.2094C>T (p.Asn698=) rs757172850
NM_000352.6(ABCC8):c.2163G>A (p.Ser721=) rs201724038
NM_000352.6(ABCC8):c.2163G>C (p.Ser721=) rs201724038
NM_000352.6(ABCC8):c.2169T>C (p.Leu723=) rs1591794603
NM_000352.6(ABCC8):c.2178A>G (p.Ala726=) rs747902103
NM_000352.6(ABCC8):c.2235C>T (p.Ser745=) rs200708414
NM_000352.6(ABCC8):c.2291+7C>A rs770152618
NM_000352.6(ABCC8):c.2291+8G>A rs748169568
NM_000352.6(ABCC8):c.234C>A (p.Thr78=) rs1591928554
NM_000352.6(ABCC8):c.2694+9del rs1564898910
NM_000352.6(ABCC8):c.2709G>A (p.Lys903=) rs1591749128
NM_000352.6(ABCC8):c.2880C>T (p.Ser960=) rs774603418
NM_000352.6(ABCC8):c.291-8C>T rs370095966
NM_000352.6(ABCC8):c.297C>T (p.Thr99=) rs906180828
NM_000352.6(ABCC8):c.3018C>T (p.Ser1006=) rs149279510
NM_000352.6(ABCC8):c.3081G>T (p.Val1027=) rs745860035
NM_000352.6(ABCC8):c.3087C>T (p.Ile1029=) rs376413488
NM_000352.6(ABCC8):c.3099G>A (p.Leu1033=) rs200693100
NM_000352.6(ABCC8):c.3111C>T (p.Thr1037=) rs201662945
NM_000352.6(ABCC8):c.3129G>A (p.Leu1043=) rs1591744434
NM_000352.6(ABCC8):c.3174C>T (p.Leu1058=) rs778240883
NM_000352.6(ABCC8):c.3203C>T (p.Thr1068Met) rs139524121
NM_000352.6(ABCC8):c.3228G>T (p.Val1076=) rs368587840
NM_000352.6(ABCC8):c.3243G>A (p.Thr1081=) rs771538281
NM_000352.6(ABCC8):c.3309G>T (p.Arg1103=) rs1321810156
NM_000352.6(ABCC8):c.3318A>G (p.Leu1106=) rs750430789
NM_000352.6(ABCC8):c.3339G>A (p.Glu1113=) rs757191246
NM_000352.6(ABCC8):c.3435C>T (p.Ser1145=) rs371089976
NM_000352.6(ABCC8):c.3513C>A (p.Ala1171=) rs778961697
NM_000352.6(ABCC8):c.3513C>T (p.Ala1171=) rs778961697
NM_000352.6(ABCC8):c.3516C>T (p.Ile1172=) rs142155036
NM_000352.6(ABCC8):c.3552G>A (p.Ala1184=) rs144207158
NM_000352.6(ABCC8):c.3573G>A (p.Leu1191=) rs1038735802
NM_000352.6(ABCC8):c.3618C>T (p.Thr1206=) rs775134825
NM_000352.6(ABCC8):c.3650+9C>A rs1591730796
NM_000352.6(ABCC8):c.3681C>T (p.Leu1227=) rs370636988
NM_000352.6(ABCC8):c.3753+10A>G rs1591718533
NM_000352.6(ABCC8):c.3754-6C>T rs1591717230
NM_000352.6(ABCC8):c.3858C>T (p.Tyr1286=) rs377045545
NM_000352.6(ABCC8):c.3868-5C>T rs1591715618
NM_000352.6(ABCC8):c.393C>T (p.Asn131=) rs372524091
NM_000352.6(ABCC8):c.3960C>T (p.Thr1320=) rs137868047
NM_000352.6(ABCC8):c.3996G>A (p.Ser1332=) rs746146690
NM_000352.6(ABCC8):c.405G>C (p.Leu135=) rs1591916038
NM_000352.6(ABCC8):c.4062C>T (p.Asp1354=) rs1591714060
NM_000352.6(ABCC8):c.4077G>A (p.Pro1359=) rs547430068
NM_000352.6(ABCC8):c.4089C>T (p.His1363=) rs1211875269
NM_000352.6(ABCC8):c.4095T>C (p.Asn1365=) rs1207446214
NM_000352.6(ABCC8):c.413-5G>C rs186946111
NM_000352.6(ABCC8):c.4140C>T (p.Thr1380=) rs574684578
NM_000352.6(ABCC8):c.4194C>T (p.Phe1398=) rs746249607
NM_000352.6(ABCC8):c.4199-6A>G rs1591710040
NM_000352.6(ABCC8):c.4227C>T (p.Ile1409=) rs146584228
NM_000352.6(ABCC8):c.4239G>A (p.Pro1413=) rs373478721
NM_000352.6(ABCC8):c.4239G>T (p.Pro1413=) rs373478721
NM_000352.6(ABCC8):c.4296C>T (p.Ser1432=) rs752222583
NM_000352.6(ABCC8):c.4360C>T (p.Leu1454=) rs544133684
NM_000352.6(ABCC8):c.4412-4T>G rs1476016104
NM_000352.6(ABCC8):c.4431C>T (p.Gly1477=) rs145673861
NM_000352.6(ABCC8):c.4464G>A (p.Leu1488=) rs374880588
NM_000352.6(ABCC8):c.4482C>T (p.Ala1494=) rs374853931
NM_000352.6(ABCC8):c.4546-4G>A rs770984647
NM_000352.6(ABCC8):c.4546-8C>T rs1273503048
NM_000352.6(ABCC8):c.4563G>T (p.Lys1521Asn) rs142272833
NM_000352.6(ABCC8):c.4581C>T (p.Phe1527=) rs773042150
NM_000352.6(ABCC8):c.45C>T (p.Tyr15=) rs758231286
NM_000352.6(ABCC8):c.4608+10C>T rs754304889
NM_000352.6(ABCC8):c.4647C>T (p.Ile1549=) rs367862706
NM_000352.6(ABCC8):c.4653G>A (p.Leu1551=) rs17846721
NM_000352.6(ABCC8):c.486C>T (p.Ile162=) rs149872185
NM_000352.6(ABCC8):c.487G>A (p.Gly163Ser) rs574487898
NM_000352.6(ABCC8):c.495G>A (p.Ser165=) rs369136858
NM_000352.6(ABCC8):c.510C>T (p.Cys170=) rs752679178
NM_000352.6(ABCC8):c.513C>T (p.Leu171=) rs767395738
NM_000352.6(ABCC8):c.546G>A (p.Leu182=) rs1591896019
NM_000352.6(ABCC8):c.552C>T (p.Leu184=) rs151211613
NM_000352.6(ABCC8):c.579+9G>A rs776165640
NM_000352.6(ABCC8):c.627C>T (p.Asp209=) rs80356640
NM_000352.6(ABCC8):c.639G>C (p.Leu213=) rs1483834388
NM_000352.6(ABCC8):c.735C>T (p.Ile245=) rs535141079
NM_000352.6(ABCC8):c.765C>T (p.Ile255=) rs753335564
NM_000352.6(ABCC8):c.813C>T (p.Asp271=) rs569222899
NM_000352.6(ABCC8):c.822+9G>A rs1007498516
NM_000352.6(ABCC8):c.951A>G (p.Pro317=) rs1591885314
NM_000352.6(ABCC8):c.954G>A (p.Leu318=) rs771014822
NM_000352.6(ABCC8):c.987G>A (p.Lys329=) rs1216809389
NM_000352.6(ABCC8):c.993C>T (p.Asn331=) rs752188418
NM_001287174.2(ABCC8):c.1630+10C>T rs188075767
NM_001287174.2(ABCC8):c.1924-10C>T rs200823913
NM_001287174.2(ABCC8):c.291-3C>T rs764107333
NM_001287174.2(ABCC8):c.3561-7G>A rs900191703
NM_001287174.2(ABCC8):c.3870+7G>A rs372198547
NM_001287174.2(ABCC8):c.413-5G>A rs186946111
NM_001287174.2(ABCC8):c.4548+13C>T rs78338172

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