ClinVar Miner

List of variants in gene ABCC8 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 42
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HGVS dbSNP gnomAD frequency
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

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