ClinVar Miner

List of variants in gene CHRNB3 studied for not specified

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_000749.5(CHRNB3):c.767A>C (p.Tyr256Ser) rs774103938 0.00032
NM_000749.5(CHRNB3):c.1124A>G (p.Lys375Arg) rs372542634 0.00020
NM_000749.5(CHRNB3):c.202G>A (p.Val68Met) rs376306516 0.00014
NM_000749.5(CHRNB3):c.655T>C (p.Ser219Pro) rs577432391 0.00011
NM_000749.5(CHRNB3):c.422T>C (p.Val141Ala) rs144291358 0.00009
NM_000749.5(CHRNB3):c.169T>C (p.Tyr57His) rs375375959 0.00003
NM_000749.5(CHRNB3):c.811G>A (p.Val271Ile) rs1173756143 0.00003
NM_000749.5(CHRNB3):c.1072T>C (p.Ser358Pro) rs761358053 0.00002
NM_000749.5(CHRNB3):c.1364A>G (p.His455Arg) rs760670573 0.00002
NM_000749.5(CHRNB3):c.313G>A (p.Val105Ile) rs377712071 0.00002
NM_000749.5(CHRNB3):c.1186G>T (p.Ala396Ser) rs1413044039 0.00001
NM_000749.5(CHRNB3):c.390G>A (p.Met130Ile) rs557808043 0.00001
NM_000749.5(CHRNB3):c.416G>A (p.Gly139Glu) rs900331287 0.00001
NM_000749.5(CHRNB3):c.53C>T (p.Ala18Val) rs1815961227 0.00001
NM_000749.5(CHRNB3):c.616G>A (p.Ala206Thr) rs576780909 0.00001
NM_000749.5(CHRNB3):c.734T>C (p.Leu245Pro) rs1172184865 0.00001
NM_000749.5(CHRNB3):c.907A>G (p.Ile303Val) rs763766498 0.00001
NM_000749.5(CHRNB3):c.1100T>C (p.Val367Ala)
NM_000749.5(CHRNB3):c.1126A>C (p.Lys376Gln) rs777983441
NM_000749.5(CHRNB3):c.1146T>A (p.Ser382Arg) rs1362048564
NM_000749.5(CHRNB3):c.1201T>C (p.Tyr401His)
NM_000749.5(CHRNB3):c.1324T>G (p.Ser442Ala)
NM_000749.5(CHRNB3):c.134G>T (p.Arg45Leu) rs755411549
NM_000749.5(CHRNB3):c.295G>A (p.Gly99Arg)
NM_000749.5(CHRNB3):c.347T>C (p.Val116Ala)
NM_000749.5(CHRNB3):c.367G>C (p.Gly123Arg)
NM_000749.5(CHRNB3):c.380G>T (p.Gly127Val)
NM_000749.5(CHRNB3):c.398T>A (p.Val133Asp)
NM_000749.5(CHRNB3):c.419C>G (p.Thr140Ser)
NM_000749.5(CHRNB3):c.469G>A (p.Val157Ile)
NM_000749.5(CHRNB3):c.499T>C (p.Cys167Arg)
NM_000749.5(CHRNB3):c.637A>G (p.Arg213Gly) rs2486834466
NM_000749.5(CHRNB3):c.655T>G (p.Ser219Ala) rs577432391
NM_000749.5(CHRNB3):c.674A>G (p.Tyr225Cys)
NM_000749.5(CHRNB3):c.682G>C (p.Val228Leu)
NM_000749.5(CHRNB3):c.691C>A (p.Arg231Ser)
NM_000749.5(CHRNB3):c.702A>C (p.Leu234Phe) rs2486834742
NM_000749.5(CHRNB3):c.70T>C (p.Ser24Pro)
NM_000749.5(CHRNB3):c.809C>T (p.Ser270Leu)
NM_000749.5(CHRNB3):c.836T>G (p.Leu279Arg)
NM_000749.5(CHRNB3):c.92C>A (p.Ala31Asp) rs1334592295
NM_000749.5(CHRNB3):c.943G>A (p.Val315Met)
NM_000749.5(CHRNB3):c.944T>C (p.Val315Ala)

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