ClinVar Miner

List of variants in gene GABRA1 reported as uncertain significance by Invitae

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Total variants: 65
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HGVS dbSNP
NM_001127644.2(GABRA1):c.1004A>T (p.Asn335Ile) rs1581220295
NM_001127644.2(GABRA1):c.1020A>C (p.Arg340Ser) rs1561587910
NM_001127644.2(GABRA1):c.1033G>A (p.Asp345Asn)
NM_001127644.2(GABRA1):c.1059+2T>C
NM_001127644.2(GABRA1):c.1070T>C (p.Val357Ala) rs749707253
NM_001127644.2(GABRA1):c.1105G>A (p.Ala369Thr) rs775344663
NM_001127644.2(GABRA1):c.1108C>A (p.Pro370Thr) rs1424508480
NM_001127644.2(GABRA1):c.1147G>A (p.Asp383Asn)
NM_001127644.2(GABRA1):c.1151C>T (p.Pro384Leu)
NM_001127644.2(GABRA1):c.1160C>T (p.Ala387Val)
NM_001127644.2(GABRA1):c.1192A>G (p.Lys398Glu)
NM_001127644.2(GABRA1):c.1207G>C (p.Glu403Gln) rs775157869
NM_001127644.2(GABRA1):c.1211C>G (p.Thr404Arg)
NM_001127644.2(GABRA1):c.1228A>G (p.Lys410Glu) rs1424659316
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.1244G>C (p.Ser415Thr)
NM_001127644.2(GABRA1):c.1253A>G (p.Lys418Arg)
NM_001127644.2(GABRA1):c.1274T>C (p.Ile425Thr)
NM_001127644.2(GABRA1):c.1297A>G (p.Ile433Val) rs1057518405
NM_001127644.2(GABRA1):c.1321_1324delinsC (p.Thr441_Tyr442delinsHis)
NM_001127644.2(GABRA1):c.1332C>G (p.Asn444Lys) rs1554087843
NM_001127644.2(GABRA1):c.1351G>A (p.Ala451Thr) rs1312439667
NM_001127644.2(GABRA1):c.1354_1356dup (p.Pro452dup)
NM_001127644.2(GABRA1):c.1358C>T (p.Thr453Ile)
NM_001127644.2(GABRA1):c.1366C>T (p.Gln456Ter)
NM_001127644.2(GABRA1):c.190C>T (p.Arg64Cys)
NM_001127644.2(GABRA1):c.217T>A (p.Phe73Ile)
NM_001127644.2(GABRA1):c.226A>G (p.Ser76Gly)
NM_001127644.2(GABRA1):c.268G>T (p.Asp90Tyr)
NM_001127644.2(GABRA1):c.296A>G (p.Asp99Gly)
NM_001127644.2(GABRA1):c.334C>T (p.Arg112Trp)
NM_001127644.2(GABRA1):c.474G>A (p.Met158Ile)
NM_001127644.2(GABRA1):c.485T>G (p.Val162Gly) rs1554085822
NM_001127644.2(GABRA1):c.498T>G (p.Cys166Trp) rs1437350481
NM_001127644.2(GABRA1):c.534T>G (p.His178Gln)
NM_001127644.2(GABRA1):c.59C>T (p.Thr20Ile) rs756553428
NM_001127644.2(GABRA1):c.602A>G (p.Glu201Gly)
NM_001127644.2(GABRA1):c.611G>A (p.Arg204His)
NM_001127644.2(GABRA1):c.634G>C (p.Gly212Arg)
NM_001127644.2(GABRA1):c.637T>A (p.Ser213Thr) rs1581207094
NM_001127644.2(GABRA1):c.638C>T (p.Ser213Leu)
NM_001127644.2(GABRA1):c.649C>A (p.Gln217Lys) rs1554086437
NM_001127644.2(GABRA1):c.653A>C (p.Tyr218Ser)
NM_001127644.2(GABRA1):c.677A>G (p.Asp226Gly)
NM_001127644.2(GABRA1):c.703+5G>A
NM_001127644.2(GABRA1):c.725C>T (p.Thr242Ile)
NM_001127644.2(GABRA1):c.74+3_74+4delinsAT
NM_001127644.2(GABRA1):c.74+6G>A
NM_001127644.2(GABRA1):c.75C>T (p.Ser25=) rs75423500
NM_001127644.2(GABRA1):c.770C>T (p.Thr257Ile)
NM_001127644.2(GABRA1):c.787A>T (p.Met263Leu) rs1561584736
NM_001127644.2(GABRA1):c.799C>A (p.Leu267Ile) rs796052492
NM_001127644.2(GABRA1):c.824A>G (p.Asn275Ser)
NM_001127644.2(GABRA1):c.850G>C (p.Val284Leu)
NM_001127644.2(GABRA1):c.859G>A (p.Val287Ile) rs796052493
NM_001127644.2(GABRA1):c.85C>T (p.Pro29Ser) rs143815396
NM_001127644.2(GABRA1):c.863C>T (p.Thr288Ile)
NM_001127644.2(GABRA1):c.881C>G (p.Thr294Arg)
NM_001127644.2(GABRA1):c.8A>G (p.Lys3Arg)
NM_001127644.2(GABRA1):c.914C>T (p.Pro305Leu)
NM_001127644.2(GABRA1):c.920T>C (p.Val307Ala) rs1581220195
NM_001127644.2(GABRA1):c.932C>T (p.Thr311Ile) rs1581220210
NM_001127644.2(GABRA1):c.94C>A (p.Gln32Lys) rs769743354
NM_001127644.2(GABRA1):c.962A>G (p.Tyr321Cys)

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