ClinVar Miner

List of variants in gene CHRNA4 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_000744.7(CHRNA4):c.1352C>T (p.Pro451Leu) rs55915440 0.00262
NM_000744.7(CHRNA4):c.1401C>T (p.Ser467=) rs45569837 0.00262
NM_000744.7(CHRNA4):c.1353G>A (p.Pro451=) rs113168860 0.00222
NM_000744.7(CHRNA4):c.1143C>T (p.Ala381=) rs75221202 0.00208
NM_000744.7(CHRNA4):c.1047G>A (p.Leu349=) rs75593857 0.00200
NM_000744.7(CHRNA4):c.1460G>A (p.Arg487Gln) rs121912280 0.00152
NM_000744.7(CHRNA4):c.77-4G>A rs201123897 0.00141
NM_000744.7(CHRNA4):c.978C>T (p.Phe326=) rs76270730 0.00122
NM_000744.7(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652 0.00080
NM_000744.7(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225 0.00070
NM_000744.7(CHRNA4):c.225C>T (p.Asp75=) rs113080067 0.00051
NM_000744.7(CHRNA4):c.1006C>T (p.Arg336Cys) rs56175056 0.00045
NM_000744.7(CHRNA4):c.1665C>T (p.Pro555=) rs199829902 0.00028
NM_000744.7(CHRNA4):c.1584G>A (p.Pro528=) rs199783192 0.00021
NM_000744.7(CHRNA4):c.1635G>A (p.Thr545=) rs121912283 0.00021
NM_000744.7(CHRNA4):c.1291C>T (p.Pro431Ser) rs201287245 0.00016
NM_000744.7(CHRNA4):c.1448G>A (p.Arg483Gln) rs55855125 0.00016
NM_000744.7(CHRNA4):c.1360G>A (p.Gly454Ser) rs78306886 0.00014
NM_000744.7(CHRNA4):c.1459C>T (p.Arg487Trp) rs200200279 0.00013
NM_000744.7(CHRNA4):c.1715A>G (p.Gln572Arg) rs113794453 0.00011
NM_000744.7(CHRNA4):c.948C>T (p.Phe316=) rs121912259 0.00011
NM_000744.7(CHRNA4):c.1228G>A (p.Val410Ile) rs121912272 0.00010
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=) rs121912253 0.00009
NM_000744.7(CHRNA4):c.852G>A (p.Ser284=) rs199741056 0.00007
NM_000744.7(CHRNA4):c.1116C>T (p.Ile372=) rs199889002 0.00006
NM_000744.7(CHRNA4):c.1815G>A (p.Met605Ile) rs774394637 0.00006
NM_000744.7(CHRNA4):c.1757C>T (p.Ser586Leu) rs200644872 0.00004
NM_000744.7(CHRNA4):c.669C>T (p.Tyr223=) rs79068736 0.00004
NM_000744.7(CHRNA4):c.1012C>G (p.His338Asp) rs200069626 0.00002
NM_000744.7(CHRNA4):c.1082C>T (p.Pro361Leu) rs267606048 0.00002
NM_000744.7(CHRNA4):c.1217C>T (p.Pro406Leu) rs777222517 0.00002
NM_000744.7(CHRNA4):c.1421C>G (p.Pro474Arg) rs199778549 0.00002
NM_000744.7(CHRNA4):c.1531G>T (p.Ala511Ser) rs200795334 0.00002
NM_000744.7(CHRNA4):c.390C>T (p.Asp130=) rs375014053 0.00002
NM_000744.7(CHRNA4):c.560C>G (p.Ala187Gly) rs200197645 0.00002
NM_000744.7(CHRNA4):c.1060C>T (p.Arg354Cys) rs758534439 0.00001
NM_000744.7(CHRNA4):c.1159G>A (p.Glu387Lys) rs534229205 0.00001
NM_000744.7(CHRNA4):c.1634C>T (p.Thr545Met) rs121912282 0.00001
NM_000744.7(CHRNA4):c.1677C>T (p.Pro559=) rs767662388 0.00001
NM_000744.7(CHRNA4):c.1696C>T (p.Arg566Trp) rs201674914 0.00001
NM_000744.7(CHRNA4):c.176C>T (p.Ser59Leu) rs775143571 0.00001
NM_000744.7(CHRNA4):c.199G>A (p.Gly67Ser) rs750325388 0.00001
NM_000744.7(CHRNA4):c.778C>A (p.Leu260Ile) rs770780958 0.00001
NM_000744.7(CHRNA4):c.1011G>A (p.Thr337=)
NM_000744.7(CHRNA4):c.1158C>T (p.Pro386=) rs45564639
NM_000744.7(CHRNA4):c.170A>G (p.Asn57Ser) rs2145408343
NM_000744.7(CHRNA4):c.1726G>C (p.Asp576His) rs537904499
NM_000744.7(CHRNA4):c.1728C>A (p.Asp576Glu)
NM_000744.7(CHRNA4):c.939C>T (p.Thr313=)
NM_000744.7(CHRNA4):c.959C>A (p.Ser320Tyr) rs776272483

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