ClinVar Miner

List of variants in gene GABRA1 reported as uncertain significance for not provided

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Total variants: 29
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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.1130C>T (p.Pro377Leu) rs751571034
NM_001127644.2(GABRA1):c.1155C>A (p.Gly385=) rs41308303
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.1283C>T (p.Pro428Leu)
NM_001127644.2(GABRA1):c.176C>T (p.Pro59Leu) rs1064796448
NM_001127644.2(GABRA1):c.187+5G>A rs368360804
NM_001127644.2(GABRA1):c.188A>C (p.Glu63Ala) rs1429109541
NM_001127644.2(GABRA1):c.335G>A (p.Arg112Gln) rs587777308
NM_001127644.2(GABRA1):c.39C>G (p.Ala13=) rs1581175017
NM_001127644.2(GABRA1):c.441G>T (p.Arg147=) rs190024862
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.560-20T>C rs202046572
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.704-10T>C rs188133840
NM_001127644.2(GABRA1):c.75-4del rs563768487
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.85C>T (p.Pro29Ser) rs143815396
NM_001127644.2(GABRA1):c.86C>T (p.Pro29Leu) rs200218956
NM_001127644.2(GABRA1):c.949A>C (p.Ile317Leu) rs796052498
NM_001127644.2(GABRA1):c.991T>A (p.Phe331Ile)

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