ClinVar Miner

List of variants in gene ABCC9 reported as likely benign for not provided

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Gene type:
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Total variants: 35
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HGVS dbSNP
NC_000012.12:g.21863322_21863324del
NC_000012.12:g.21872489del
NM_005691.3(ABCC9):c.1071T>A (p.Leu357=)
NM_005691.3(ABCC9):c.1165-54T>C
NM_005691.3(ABCC9):c.1660-276C>A
NM_005691.3(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969
NM_005691.3(ABCC9):c.1912-12T>C
NM_005691.3(ABCC9):c.2019+85T>A
NM_005691.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2424+78G>A
NM_005691.3(ABCC9):c.2506-301G>T
NM_005691.3(ABCC9):c.2866+171T>A
NM_005691.3(ABCC9):c.3096+100A>T
NM_005691.3(ABCC9):c.3097-42T>C
NM_005691.3(ABCC9):c.3473+112C>T
NM_005691.3(ABCC9):c.3474-93A>G
NM_005691.3(ABCC9):c.3567-180A>G
NM_005691.3(ABCC9):c.3567-197T>A
NM_005691.3(ABCC9):c.3567-20C>T
NM_005691.3(ABCC9):c.363T>C (p.Tyr121=)
NM_005691.3(ABCC9):c.3772-250T>C
NM_005691.3(ABCC9):c.3772-65C>T
NM_005691.3(ABCC9):c.4023+327A>G
NM_005691.3(ABCC9):c.4211+123A>T
NM_005691.3(ABCC9):c.4389T>C (p.Phe1463=)
NM_005691.3(ABCC9):c.444A>G (p.Lys148=)
NM_005691.3(ABCC9):c.4570T>A (p.Leu1524Ile) rs139703258
NM_005691.3(ABCC9):c.4571T>A (p.Leu1524Ter) rs150631550
NM_005691.3(ABCC9):c.4572_4573insT (p.Val1525fs) rs761784169
NM_005691.3(ABCC9):c.573+12A>C
NM_005691.3(ABCC9):c.639G>A (p.Val213=)
NM_020297.3(ABCC9):c.4512+1094A>C
NM_020297.3(ABCC9):c.4638C>T (p.Arg1546=)

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