ClinVar Miner

List of variants in gene GABRA1 studied for not provided

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Total variants: 81
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HGVS dbSNP
GRCh37/hg19 5q34(chr5:161249860-161316596)x1
NM_001127644.2(GABRA1):c.*2T>A rs762836110
NM_001127644.2(GABRA1):c.-15-9A>T rs770530140
NM_001127644.2(GABRA1):c.-16+15G>A rs1581172079
NM_001127644.2(GABRA1):c.1060-10del rs1581221506
NM_001127644.2(GABRA1):c.1060-245C>T rs4144483
NM_001127644.2(GABRA1):c.1104C>T (p.Tyr368=) rs771832995
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.1206C>T (p.Pro402=) rs541335259
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.1229A>G (p.Lys410Arg) rs376031361
NM_001127644.2(GABRA1):c.1234A>T (p.Thr412Ser) rs1229633395
NM_001127644.2(GABRA1):c.1263A>T (p.Arg421=) rs1581221881
NM_001127644.2(GABRA1):c.1283C>T (p.Pro428Leu)
NM_001127644.2(GABRA1):c.1313A>G (p.Tyr438Cys)
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.156T>C (p.Gly52=) rs1129647
NM_001127644.2(GABRA1):c.176C>T (p.Pro59Leu) rs1064796448
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.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.297T>C (p.Asp99=) rs750394365
NM_001127644.2(GABRA1):c.335G>A (p.Arg112Gln) rs587777308
NM_001127644.2(GABRA1):c.384C>T (p.Phe128=) rs1219475284
NM_001127644.2(GABRA1):c.39C>G (p.Ala13=) rs1581175017
NM_001127644.2(GABRA1):c.439C>T (p.Arg147Trp) rs139163545
NM_001127644.2(GABRA1):c.441G>T (p.Arg147=) rs190024862
NM_001127644.2(GABRA1):c.45C>T (p.Ile15=) rs759784427
NM_001127644.2(GABRA1):c.477-5T>C rs779231183
NM_001127644.2(GABRA1):c.484G>A (p.Val162Met) rs796052499
NM_001127644.2(GABRA1):c.499C>T (p.Pro167Ser) rs1581200203
NM_001127644.2(GABRA1):c.501G>A (p.Pro167=) rs200750234
NM_001127644.2(GABRA1):c.559+80G>A rs4260711
NM_001127644.2(GABRA1):c.560-20T>C rs202046572
NM_001127644.2(GABRA1):c.560-261A>G rs4921199
NM_001127644.2(GABRA1):c.560-9T>C rs1581207011
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.640C>A (p.Arg214Ser) rs727503940
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.699T>C (p.Ser233=) rs756876744
NM_001127644.2(GABRA1):c.703+295A>G rs12658807
NM_001127644.2(GABRA1):c.703+45T>G rs11135172
NM_001127644.2(GABRA1):c.704-10T>C rs188133840
NM_001127644.2(GABRA1):c.704-247T>C rs41275317
NM_001127644.2(GABRA1):c.74+10C>T rs557887445
NM_001127644.2(GABRA1):c.75-4del rs563768487
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.799C>A (p.Leu267Ile) rs796052492
NM_001127644.2(GABRA1):c.829G>C (p.Glu277Gln) rs1064797317
NM_001127644.2(GABRA1):c.851T>C (p.Val284Ala) rs794727962
NM_001127644.2(GABRA1):c.857-2A>G rs1313965409
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.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.966C>T (p.Ala322=) rs201133616
NM_001127644.2(GABRA1):c.96A>G (p.Gln32=) rs76224028
NM_001127644.2(GABRA1):c.973T>C (p.Phe325Leu) rs1064794681
NM_001127644.2(GABRA1):c.991T>A (p.Phe331Ile)

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