ClinVar Miner

List of variants in gene CHRNA4 reported as likely benign for not provided

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Total variants: 42
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HGVS dbSNP
NC_000020.11:g.63351236_63351241del rs1279429508
NM_000744.6(CHRNA4):c.1194C>T (p.Thr398=) rs752592838
NM_000744.6(CHRNA4):c.1209G>A (p.Pro403=) rs2229959
NM_000744.6(CHRNA4):c.1221C>T (p.Ser407=) rs1601473794
NM_000744.6(CHRNA4):c.1337C>T (p.Pro446Leu) rs769897766
NM_000744.6(CHRNA4):c.1395C>T (p.Ser465=) rs748016098
NM_000744.6(CHRNA4):c.1779C>T (p.Tyr593=) rs201347598
NM_000744.6(CHRNA4):c.369C>T (p.Ile123=) rs1334588457
NM_000744.6(CHRNA4):c.384-194G>A rs74879482
NM_000744.6(CHRNA4):c.384-199T>G rs75683226
NM_000744.6(CHRNA4):c.384-207T>C rs74934614
NM_000744.6(CHRNA4):c.384-208G>A rs8124042
NM_000744.6(CHRNA4):c.414G>A (p.Leu138=) rs769287364
NM_000744.6(CHRNA4):c.77-102G>C rs140380399
NM_000744.6(CHRNA4):c.77-235C>T rs533457282
NM_000744.6(CHRNA4):c.787C>T (p.Leu263=) rs76830527
NM_000744.6(CHRNA4):c.957G>A (p.Leu319=) rs761872673
NM_000744.6(CHRNA4):c.95C>A (p.Thr32Asn) rs200601170
NM_000744.6(CHRNA4):c.987C>T (p.Asn329=) rs572366184
NM_000744.7(CHRNA4):c.1116C>T (p.Ile372=) rs199889002
NM_000744.7(CHRNA4):c.1228G>A (p.Val410Ile) rs121912272
NM_000744.7(CHRNA4):c.1291C>T (p.Pro431Ser)
NM_000744.7(CHRNA4):c.1352C>T (p.Pro451Leu) rs55915440
NM_000744.7(CHRNA4):c.1360G>A (p.Gly454Ser) rs78306886
NM_000744.7(CHRNA4):c.1417A>G (p.Ser473Gly) rs1555837484
NM_000744.7(CHRNA4):c.1494C>T (p.Ala498=) rs137860047
NM_000744.7(CHRNA4):c.1551G>A (p.Ser517=) rs201441215
NM_000744.7(CHRNA4):c.1635G>A (p.Thr545=) rs121912283
NM_000744.7(CHRNA4):c.1646G>A (p.Arg549His) rs768292011
NM_000744.7(CHRNA4):c.1658C>T (p.Ala553Val) rs762808071
NM_000744.7(CHRNA4):c.1677C>T (p.Pro559=) rs767662388
NM_000744.7(CHRNA4):c.1824C>T (p.Ile608=) rs748027182
NM_000744.7(CHRNA4):c.1860G>A (p.Pro620=) rs202203317
NM_000744.7(CHRNA4):c.1867C>T (p.Leu623=) rs878854142
NM_000744.7(CHRNA4):c.501C>T (p.Phe167=) rs374602963
NM_000744.7(CHRNA4):c.510C>T (p.Phe170=) rs121912247
NM_000744.7(CHRNA4):c.537C>T (p.Phe179=) rs747499031
NM_000744.7(CHRNA4):c.591C>T (p.Arg197=) rs776092779
NM_000744.7(CHRNA4):c.712G>A (p.Val238Ile) rs745790876
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=) rs121912253
NM_000744.7(CHRNA4):c.900A>G (p.Ser300=) rs878854143
NM_000744.7(CHRNA4):c.964G>A (p.Val322Ile) rs779790555

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