ClinVar Miner

List of variants in gene GABRA1 reported as likely benign by GeneDx

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Gene type:
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Total variants: 42
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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.-15-23T>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.-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.-258T>C rs183280626
NM_001127644.2(GABRA1):c.-263A>G rs763127240
NM_001127644.2(GABRA1):c.-4C>T rs375475234
NM_001127644.2(GABRA1):c.1146C>T (p.Gly382=) rs79593368
NM_001127644.2(GABRA1):c.11G>A (p.Ser4Asn) rs796052487
NM_001127644.2(GABRA1):c.1299C>A (p.Ile433=) rs1340729708
NM_001127644.2(GABRA1):c.187+16G>A rs1554084016
NM_001127644.2(GABRA1):c.198C>T (p.Thr66=) rs770208588
NM_001127644.2(GABRA1):c.255+13T>C rs1554084940
NM_001127644.2(GABRA1):c.261T>C (p.Tyr87=) rs1057523723
NM_001127644.2(GABRA1):c.27C>A (p.Asp9Glu) rs113886269
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.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.559+19A>G rs1554085838
NM_001127644.2(GABRA1):c.612C>T (p.Arg204=) rs374616425
NM_001127644.2(GABRA1):c.703+9G>T rs768499906
NM_001127644.2(GABRA1):c.704-17T>G rs115043829
NM_001127644.2(GABRA1):c.729T>C (p.His243=) rs772218052
NM_001127644.2(GABRA1):c.74+19A>G rs370522819
NM_001127644.2(GABRA1):c.78T>C (p.Tyr26=) rs779666888
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.873C>T (p.Leu291=) rs777911034
NM_001127644.2(GABRA1):c.87G>A (p.Pro29=) rs374399356

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