ClinVar Miner

List of variants in gene CHRNA4 reported as likely benign by Ambry Genetics

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Total variants: 34
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HGVS dbSNP
NM_000744.6(CHRNA4):c.1006C>T (p.Arg336Cys) rs56175056
NM_000744.6(CHRNA4):c.1047G>A (p.Leu349=) rs75593857
NM_000744.6(CHRNA4):c.1053C>T (p.Ile351=) rs61737042
NM_000744.6(CHRNA4):c.1143C>T (p.Ala381=) rs75221202
NM_000744.6(CHRNA4):c.1191C>T (p.Gly397=) rs1568808988
NM_000744.6(CHRNA4):c.1203G>C (p.Leu401=) rs56142348
NM_000744.6(CHRNA4):c.1249G>A (p.Glu417Lys) rs369269532
NM_000744.6(CHRNA4):c.1353G>A (p.Pro451=) rs113168860
NM_000744.6(CHRNA4):c.1360G>A (p.Gly454Ser) rs78306886
NM_000744.6(CHRNA4):c.138C>T (p.Ser46=) rs200705061
NM_000744.6(CHRNA4):c.1401C>T (p.Ser467=) rs45569837
NM_000744.6(CHRNA4):c.1415C>T (p.Ser472Phe) rs534477048
NM_000744.6(CHRNA4):c.1431G>A (p.Ala477=) rs80307076
NM_000744.6(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225
NM_000744.6(CHRNA4):c.1460G>A (p.Arg487Gln) rs121912280
NM_000744.6(CHRNA4):c.1500C>T (p.Pro500=) rs201391859
NM_000744.6(CHRNA4):c.1538G>A (p.Arg513His) rs868845088
NM_000744.6(CHRNA4):c.1550C>T (p.Ser517Leu) rs45622132
NM_000744.6(CHRNA4):c.1551G>A (p.Ser517=) rs201441215
NM_000744.6(CHRNA4):c.1584G>A (p.Pro528=) rs199783192
NM_000744.6(CHRNA4):c.1596A>G (p.Thr532=) rs533213338
NM_000744.6(CHRNA4):c.1662G>A (p.Pro554=) rs121912284
NM_000744.6(CHRNA4):c.225C>T (p.Asp75=) rs113080067
NM_000744.6(CHRNA4):c.258C>T (p.Asn86=) rs140239470
NM_000744.6(CHRNA4):c.274G>C (p.Glu92Gln) rs146651027
NM_000744.6(CHRNA4):c.402G>A (p.Ala134=) rs201488442
NM_000744.6(CHRNA4):c.492C>T (p.Asp164=) rs200259564
NM_000744.6(CHRNA4):c.681C>A (p.Ala227=) rs45588436
NM_000744.6(CHRNA4):c.77-4G>A rs201123897
NM_000744.6(CHRNA4):c.852G>A (p.Ser284=) rs199741056
NM_000744.6(CHRNA4):c.879C>T (p.Thr293=) rs371527699
NM_000744.6(CHRNA4):c.931C>T (p.Leu311=) rs767662811
NM_000744.6(CHRNA4):c.978C>T (p.Phe326=) rs76270730
NM_000744.6(CHRNA4):c.99G>C (p.Arg33=) rs539718301

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