ClinVar Miner

List of variants in gene GABRA1 reported by GeneDx

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Total variants: 100
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HGVS dbSNP
NM_000806.5(GABRA1):c.-248+10C>T rs1050530276
NM_001127644.2(GABRA1):c.*2T>A rs762836110
NM_001127644.2(GABRA1):c.-15-20C>T rs555933670
NM_001127644.2(GABRA1):c.-15-23T>A rs534129599
NM_001127644.2(GABRA1):c.-15-25G>T rs200321984
NM_001127644.2(GABRA1):c.-15-9A>T rs770530140
NM_001127644.2(GABRA1):c.-16+15G>A rs1581172079
NM_001127644.2(GABRA1):c.-16+18C>G rs978912528
NM_001127644.2(GABRA1):c.-16+8C>A rs138671319
NM_001127644.2(GABRA1):c.-19T>C rs1057521883
NM_001127644.2(GABRA1):c.-19_-18del rs1064794832
NM_001127644.2(GABRA1):c.-241A>T rs1402044979
NM_001127644.2(GABRA1):c.-243A>G rs1554083390
NM_001127644.2(GABRA1):c.-247C>T rs1043312870
NM_001127644.2(GABRA1):c.-24G>C rs981975825
NM_001127644.2(GABRA1):c.-257T>C rs587780946
NM_001127644.2(GABRA1):c.-258T>C rs183280626
NM_001127644.2(GABRA1):c.-263A>G rs763127240
NM_001127644.2(GABRA1):c.-4C>T rs375475234
NM_001127644.2(GABRA1):c.1060-15T>C rs773638322
NM_001127644.2(GABRA1):c.1060-245C>T rs4144483
NM_001127644.2(GABRA1):c.1086T>C (p.Ile362=) rs187648029
NM_001127644.2(GABRA1):c.1130C>T (p.Pro377Leu) rs751571034
NM_001127644.2(GABRA1):c.1146C>T (p.Gly382=) rs79593368
NM_001127644.2(GABRA1):c.1155C>A (p.Gly385=) rs41308303
NM_001127644.2(GABRA1):c.11G>A (p.Ser4Asn) rs796052487
NM_001127644.2(GABRA1):c.1207G>C (p.Glu403Gln) rs775157869
NM_001127644.2(GABRA1):c.1225C>T (p.Pro409Ser) rs139793542
NM_001127644.2(GABRA1):c.1234A>T (p.Thr412Ser) rs1229633395
NM_001127644.2(GABRA1):c.1284G>A (p.Pro428=) rs74873701
NM_001127644.2(GABRA1):c.1297A>G (p.Ile433Val) rs1057518405
NM_001127644.2(GABRA1):c.1299C>A (p.Ile433=) rs1340729708
NM_001127644.2(GABRA1):c.1323G>A (p.Thr441=) rs138259457
NM_001127644.2(GABRA1):c.1350A>G (p.Lys450=) rs142385746
NM_001127644.2(GABRA1):c.176C>T (p.Pro59Leu) rs1064796448
NM_001127644.2(GABRA1):c.187+16G>A rs1554084016
NM_001127644.2(GABRA1):c.187+5G>A rs368360804
NM_001127644.2(GABRA1):c.188-42C>T rs41304896
NM_001127644.2(GABRA1):c.188A>C (p.Glu63Ala) rs1429109541
NM_001127644.2(GABRA1):c.198C>T (p.Thr66=) rs770208588
NM_001127644.2(GABRA1):c.255+12C>T rs144727170
NM_001127644.2(GABRA1):c.255+13T>C rs1554084940
NM_001127644.2(GABRA1):c.255+285C>T rs56873080
NM_001127644.2(GABRA1):c.256-201A>T rs72819308
NM_001127644.2(GABRA1):c.256-221A>G rs78679936
NM_001127644.2(GABRA1):c.256-2A>G rs1064795805
NM_001127644.2(GABRA1):c.261T>C (p.Tyr87=) rs1057523723
NM_001127644.2(GABRA1):c.268G>C (p.Asp90His) rs796052488
NM_001127644.2(GABRA1):c.27C>A (p.Asp9Glu) rs113886269
NM_001127644.2(GABRA1):c.335G>A (p.Arg112Gln) rs587777308
NM_001127644.2(GABRA1):c.378A>G (p.Thr126=) rs756299135
NM_001127644.2(GABRA1):c.414C>T (p.Asn138=) rs1057522080
NM_001127644.2(GABRA1):c.441G>T (p.Arg147=) rs190024862
NM_001127644.2(GABRA1):c.453T>C (p.Asp151=) rs1308271547
NM_001127644.2(GABRA1):c.45C>T (p.Ile15=) rs759784427
NM_001127644.2(GABRA1):c.476+19C>T rs1057522828
NM_001127644.2(GABRA1):c.477-6C>T rs1057522459
NM_001127644.2(GABRA1):c.478C>T (p.Leu160=) rs1269683161
NM_001127644.2(GABRA1):c.484G>A (p.Val162Met) rs796052499
NM_001127644.2(GABRA1):c.501G>A (p.Pro167=) rs200750234
NM_001127644.2(GABRA1):c.559+19A>G rs1554085838
NM_001127644.2(GABRA1):c.559+80G>A rs4260711
NM_001127644.2(GABRA1):c.560-261A>G rs4921199
NM_001127644.2(GABRA1):c.59C>T (p.Thr20Ile) rs756553428
NM_001127644.2(GABRA1):c.612C>T (p.Arg204=) rs374616425
NM_001127644.2(GABRA1):c.633T>C (p.Asp211=) rs587780947
NM_001127644.2(GABRA1):c.640C>T (p.Arg214Cys) rs727503940
NM_001127644.2(GABRA1):c.641G>A (p.Arg214His) rs886039373
NM_001127644.2(GABRA1):c.703+295A>G rs12658807
NM_001127644.2(GABRA1):c.703+45T>G rs11135172
NM_001127644.2(GABRA1):c.703+9G>T rs768499906
NM_001127644.2(GABRA1):c.704-17T>G rs115043829
NM_001127644.2(GABRA1):c.704-247T>C rs41275317
NM_001127644.2(GABRA1):c.729T>C (p.His243=) rs772218052
NM_001127644.2(GABRA1):c.74+19A>G rs370522819
NM_001127644.2(GABRA1):c.752G>A (p.Gly251Asp) rs1064793933
NM_001127644.2(GABRA1):c.788T>A (p.Met263Lys) rs796052491
NM_001127644.2(GABRA1):c.78T>C (p.Tyr26=) rs779666888
NM_001127644.2(GABRA1):c.799C>A (p.Leu267Ile) rs796052492
NM_001127644.2(GABRA1):c.831G>A (p.Glu277=) rs764666718
NM_001127644.2(GABRA1):c.834T>C (p.Ser278=) rs749956729
NM_001127644.2(GABRA1):c.846A>G (p.Arg282=) rs139467768
NM_001127644.2(GABRA1):c.851T>C (p.Val284Ala) rs794727962
NM_001127644.2(GABRA1):c.859G>A (p.Val287Ile) rs796052493
NM_001127644.2(GABRA1):c.859G>T (p.Val287Leu) rs796052493
NM_001127644.2(GABRA1):c.85C>T (p.Pro29Ser) rs143815396
NM_001127644.2(GABRA1):c.868G>A (p.Val290Met) rs796052494
NM_001127644.2(GABRA1):c.86C>T (p.Pro29Leu) rs200218956
NM_001127644.2(GABRA1):c.873C>T (p.Leu291=) rs777911034
NM_001127644.2(GABRA1):c.87G>A (p.Pro29=) rs374399356
NM_001127644.2(GABRA1):c.881C>T (p.Thr294Ile) rs796052495
NM_001127644.2(GABRA1):c.884C>T (p.Thr295Ile) rs796052496
NM_001127644.2(GABRA1):c.891C>G (p.Ser297Arg) rs796052497
NM_001127644.2(GABRA1):c.923C>A (p.Ala308Asp) rs1554087620
NM_001127644.2(GABRA1):c.934G>A (p.Ala312Thr) rs1131691884
NM_001127644.2(GABRA1):c.940G>A (p.Asp314Asn) rs1064795283
NM_001127644.2(GABRA1):c.949A>C (p.Ile317Leu) rs796052498
NM_001127644.2(GABRA1):c.94C>T (p.Gln32Ter) rs769743354
NM_001127644.2(GABRA1):c.954C>T (p.Ala318=) rs551045474
NM_001127644.2(GABRA1):c.973T>C (p.Phe325Leu) rs1064794681

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