ClinVar Miner

List of variants in gene COMT reported as drug response

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_000754.4(COMT):c.186C>T (p.His62=) rs4633 0.44697
NM_000754.4(COMT):c.472G>A (p.Val158Met) rs4680 0.44044
NM_000754.4(COMT):c.289+90A>G rs2239393 0.39046
NM_000754.4(COMT):c.408C>G (p.Leu136=) rs4818 0.32165
NM_000754.4(COMT):c.615+75G>C rs4646315 0.17853
NM_000754.4(COMT):c.219G>A (p.Gln73=) rs740602 0.05987
NM_000754.4(COMT):c.597G>A (p.Pro199=) rs769224 0.04486
NM_000754.4(COMT):c.1-303T>C rs11569716 0.03465
NM_000754.4(COMT):c.214G>T (p.Ala72Ser) rs6267 0.01144
NM_000754.4(COMT):c.289+17C>T rs544846648 0.00004
NM_000754.4(COMT):c.1-325G>A rs1393666377 0.00003
NM_000754.4(COMT):c.15G>A (p.Pro5=) rs561536243 0.00003
NM_000754.4(COMT):c.484-26G>A rs754436726 0.00003
NM_000754.4(COMT):c.165G>A (p.Lys55=) rs1601527185 0.00002
NM_000754.4(COMT):c.290-28C>T rs754397556 0.00002
NM_000754.4(COMT):c.14C>T (p.Pro5Leu) rs1160435070 0.00001
NM_000754.4(COMT):c.290-3C>T rs1428959883 0.00001
NM_000754.4(COMT):c.503C>T (p.Ala168Val) rs201225516 0.00001
NM_000754.4(COMT):c.-1+14C>T rs972946462
NM_000754.4(COMT):c.-1+43C>A rs1601525317
NM_000754.4(COMT):c.-162T>G rs1601501281
NM_000754.4(COMT):c.-85C>T rs1601525100
NM_000754.4(COMT):c.-91-25C>A rs1601525073
NM_000754.4(COMT):c.-91-26T>A rs1601525072
NM_000754.4(COMT):c.-91-30A>G rs1601525066
NM_000754.4(COMT):c.-91-32T>G rs1601525062
NM_000754.4(COMT):c.-91-9570G>A rs1601512807
NM_000754.4(COMT):c.-91-9583G>C rs1601512790
NM_000754.4(COMT):c.-92+9009A>T rs1601511512
NM_000754.4(COMT):c.-92+9012G>A rs1601511531
NM_000754.4(COMT):c.-92+9013C>G rs1601511537
NM_000754.4(COMT):c.-92+9015T>C rs1601511546
NM_000754.4(COMT):c.-92+9601T>G rs1601512573
NM_000754.4(COMT):c.-92+9602G>A rs1601512579
NM_000754.4(COMT):c.-92+9604C>A rs1601512585
NM_000754.4(COMT):c.-92+9605T>C rs1601512593
NM_000754.4(COMT):c.-92+9606C>A rs1601512599
NM_000754.4(COMT):c.-92+9607C>A rs1601512609
NM_000754.4(COMT):c.-92+9616C>T rs1601512631
NM_000754.4(COMT):c.-92+9619G>A rs144623972
NM_000754.4(COMT):c.-92+9635A>T rs1601512664
NM_000754.4(COMT):c.1-189C>A rs1601526514
NM_000754.4(COMT):c.1-241A>T rs1601526452
NM_000754.4(COMT):c.1-319G>A rs1601526354
NM_000754.4(COMT):c.1-326C>A rs887838460
NM_000754.4(COMT):c.1-327C>T rs1601526328
NM_000754.4(COMT):c.1-6C>T rs1601526839
NM_000754.4(COMT):c.17C>T (p.Pro6Leu) rs1601526877
NM_000754.4(COMT):c.231G>A (p.Glu77=) rs1601527383
NM_000754.4(COMT):c.243C>A (p.Thr81=) rs1601527404
NM_000754.4(COMT):c.268A>T (p.Met90Leu) rs373611092
NM_000754.4(COMT):c.280G>T (p.Asp94Tyr) rs76452330
NM_000754.4(COMT):c.289+26A>G rs1601527641
NM_000754.4(COMT):c.289+36C>T rs1601527677
NM_000754.4(COMT):c.289+85A>G rs1601527752
NM_000754.4(COMT):c.289+89C>T rs1601527756
NM_000754.4(COMT):c.290-27C>A rs778498490
NM_000754.4(COMT):c.290-29A>C rs1601528913
NM_000754.4(COMT):c.290-30C>A rs1374067391
NM_000754.4(COMT):c.334C>T (p.Leu112=) rs1601529164
NM_000754.4(COMT):c.350C>T (p.Ala117Val) rs1601529201
NM_000754.4(COMT):c.375C>T (p.Arg125=) rs1223964672
NM_000754.4(COMT):c.390G>C (p.Leu130=) rs1601529307
NM_000754.4(COMT):c.459G>A (p.Val153=) rs1601529532
NM_000754.4(COMT):c.484-103C>T rs1601530120
NM_000754.4(COMT):c.484-107T>G rs1337529868
NM_000754.4(COMT):c.484-21C>T rs1601530351
NM_000754.4(COMT):c.484-30G>A rs1601530294
NM_000754.4(COMT):c.484-34del rs1601530284
NM_000754.4(COMT):c.484-87C>G rs147863086
NM_000754.4(COMT):c.97C>T (p.Leu33=) rs1601527054

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