ClinVar Miner

List of variants in gene GABRA1 reported by Invitae

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Total variants: 164
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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.1026T>C (p.Tyr342=)
NM_001127644.2(GABRA1):c.1033G>A (p.Asp345Asn)
NM_001127644.2(GABRA1):c.1045G>A (p.Val349Met)
NM_001127644.2(GABRA1):c.1059+2T>C
NM_001127644.2(GABRA1):c.1059+8C>A rs758699164
NM_001127644.2(GABRA1):c.1060-10del rs1581221506
NM_001127644.2(GABRA1):c.1065G>A (p.Lys355=) rs1554087785
NM_001127644.2(GABRA1):c.1070T>C (p.Val357Ala) rs749707253
NM_001127644.2(GABRA1):c.1079C>A (p.Pro360His)
NM_001127644.2(GABRA1):c.1079C>T (p.Pro360Leu)
NM_001127644.2(GABRA1):c.1086T>C (p.Ile362=) rs187648029
NM_001127644.2(GABRA1):c.1104C>T (p.Tyr368=) rs771832995
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.1146C>T (p.Gly382=) rs79593368
NM_001127644.2(GABRA1):c.1147G>A (p.Asp383Asn)
NM_001127644.2(GABRA1):c.1151C>T (p.Pro384Leu)
NM_001127644.2(GABRA1):c.1152G>A (p.Pro384=)
NM_001127644.2(GABRA1):c.1155C>A (p.Gly385=) rs41308303
NM_001127644.2(GABRA1):c.1156T>G (p.Leu386Val)
NM_001127644.2(GABRA1):c.1160C>T (p.Ala387Val)
NM_001127644.2(GABRA1):c.1179A>C (p.Ala393=)
NM_001127644.2(GABRA1):c.1192A>G (p.Lys398Glu)
NM_001127644.2(GABRA1):c.11G>A (p.Ser4Asn) rs796052487
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.1211C>G (p.Thr404Arg)
NM_001127644.2(GABRA1):c.1218A>G (p.Pro406=)
NM_001127644.2(GABRA1):c.1225C>T (p.Pro409Ser) rs139793542
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.124T>C (p.Phe42Leu)
NM_001127644.2(GABRA1):c.1253A>G (p.Lys418Arg)
NM_001127644.2(GABRA1):c.1257T>C (p.Ile419=)
NM_001127644.2(GABRA1):c.1261C>A (p.Arg421=)
NM_001127644.2(GABRA1):c.1263A>T (p.Arg421=) rs1581221881
NM_001127644.2(GABRA1):c.1274T>C (p.Ile425Thr)
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.1321_1324delinsC (p.Thr441_Tyr442delinsHis)
NM_001127644.2(GABRA1):c.1323G>A (p.Thr441=) rs138259457
NM_001127644.2(GABRA1):c.1332C>G (p.Asn444Lys) rs1554087843
NM_001127644.2(GABRA1):c.1337A>G (p.Glu446Gly)
NM_001127644.2(GABRA1):c.1350A>G (p.Lys450=) rs142385746
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.148C>T (p.Leu50=)
NM_001127644.2(GABRA1):c.150A>G (p.Leu50=) rs1006797468
NM_001127644.2(GABRA1):c.156T>C (p.Gly52=) rs1129647
NM_001127644.2(GABRA1):c.190C>T (p.Arg64Cys)
NM_001127644.2(GABRA1):c.197C>A (p.Thr66Asn)
NM_001127644.2(GABRA1):c.198C>T (p.Thr66=) rs770208588
NM_001127644.2(GABRA1):c.201A>G (p.Glu67=)
NM_001127644.2(GABRA1):c.216C>T (p.Ile72=) rs200716712
NM_001127644.2(GABRA1):c.217T>A (p.Phe73Ile)
NM_001127644.2(GABRA1):c.219C>T (p.Phe73=)
NM_001127644.2(GABRA1):c.226A>G (p.Ser76Gly)
NM_001127644.2(GABRA1):c.231C>T (p.Phe77=) rs566224462
NM_001127644.2(GABRA1):c.237C>T (p.Pro79=) rs536603724
NM_001127644.2(GABRA1):c.261T>C (p.Tyr87=) rs1057523723
NM_001127644.2(GABRA1):c.268G>T (p.Asp90Tyr)
NM_001127644.2(GABRA1):c.27C>A (p.Asp9Glu) rs113886269
NM_001127644.2(GABRA1):c.28T>C (p.Cys10Arg)
NM_001127644.2(GABRA1):c.296A>G (p.Asp99Gly)
NM_001127644.2(GABRA1):c.297T>C (p.Asp99=) rs750394365
NM_001127644.2(GABRA1):c.303G>A (p.Arg101=)
NM_001127644.2(GABRA1):c.321T>A (p.Pro107=)
NM_001127644.2(GABRA1):c.32T>C (p.Leu11Pro)
NM_001127644.2(GABRA1):c.334C>T (p.Arg112Trp)
NM_001127644.2(GABRA1):c.335G>A (p.Arg112Gln) rs587777308
NM_001127644.2(GABRA1):c.33T>C (p.Leu11=) rs766418049
NM_001127644.2(GABRA1):c.348A>G (p.Leu116=)
NM_001127644.2(GABRA1):c.372G>A (p.Pro124=) rs1378731581
NM_001127644.2(GABRA1):c.408C>T (p.Ala136=)
NM_001127644.2(GABRA1):c.422T>G (p.Met141Arg)
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.453T>C (p.Asp151=) rs1308271547
NM_001127644.2(GABRA1):c.459C>T (p.Thr153=)
NM_001127644.2(GABRA1):c.45C>T (p.Ile15=) rs759784427
NM_001127644.2(GABRA1):c.474G>A (p.Met158Ile)
NM_001127644.2(GABRA1):c.476+2T>A
NM_001127644.2(GABRA1):c.477-5T>C rs779231183
NM_001127644.2(GABRA1):c.485T>G (p.Val162Gly) rs1554085822
NM_001127644.2(GABRA1):c.48C>T (p.Leu16=) rs1554083720
NM_001127644.2(GABRA1):c.498T>G (p.Cys166Trp) rs1437350481
NM_001127644.2(GABRA1):c.501G>A (p.Pro167=) rs200750234
NM_001127644.2(GABRA1):c.531C>T (p.Ala177=) rs747452052
NM_001127644.2(GABRA1):c.534T>G (p.His178Gln)
NM_001127644.2(GABRA1):c.560-9T>C rs1581207011
NM_001127644.2(GABRA1):c.576A>G (p.Ala192=) rs1319609279
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.612C>T (p.Arg204=) rs374616425
NM_001127644.2(GABRA1):c.633T>C (p.Asp211=) rs587780947
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.640C>T (p.Arg214Cys) rs727503940
NM_001127644.2(GABRA1):c.641G>A (p.Arg214His) rs886039373
NM_001127644.2(GABRA1):c.649C>A (p.Gln217Lys) rs1554086437
NM_001127644.2(GABRA1):c.653A>C (p.Tyr218Ser)
NM_001127644.2(GABRA1):c.672A>G (p.Thr224=) rs372742479
NM_001127644.2(GABRA1):c.677A>G (p.Asp226Gly)
NM_001127644.2(GABRA1):c.699T>C (p.Ser233=) rs756876744
NM_001127644.2(GABRA1):c.703+5G>A
NM_001127644.2(GABRA1):c.703+8C>A rs376693195
NM_001127644.2(GABRA1):c.703+8C>T
NM_001127644.2(GABRA1):c.704-10T>C rs188133840
NM_001127644.2(GABRA1):c.725C>T (p.Thr242Ile)
NM_001127644.2(GABRA1):c.732C>T (p.Phe244=) rs1581215256
NM_001127644.2(GABRA1):c.74+10C>T rs557887445
NM_001127644.2(GABRA1):c.74+3_74+4delinsAT
NM_001127644.2(GABRA1):c.74+6G>A
NM_001127644.2(GABRA1):c.74+9A>T rs41275339
NM_001127644.2(GABRA1):c.753C>T (p.Gly251=)
NM_001127644.2(GABRA1):c.756C>T (p.Tyr252=) rs775895535
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.78T>C (p.Tyr26=) rs779666888
NM_001127644.2(GABRA1):c.799C>A (p.Leu267Ile) rs796052492
NM_001127644.2(GABRA1):c.799C>T (p.Leu267Phe)
NM_001127644.2(GABRA1):c.824A>G (p.Asn275Ser)
NM_001127644.2(GABRA1):c.825C>A (p.Asn275Lys)
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.834T>G (p.Ser278=)
NM_001127644.2(GABRA1):c.840A>G (p.Pro280=)
NM_001127644.2(GABRA1):c.846A>G (p.Arg282=) rs139467768
NM_001127644.2(GABRA1):c.850G>C (p.Val284Leu)
NM_001127644.2(GABRA1):c.856+8C>T rs1554087151
NM_001127644.2(GABRA1):c.857-2A>G rs1313965409
NM_001127644.2(GABRA1):c.857-8C>T rs752572964
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.865A>G (p.Thr289Ala)
NM_001127644.2(GABRA1):c.869_888del (p.Val290fs) rs1561587715
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>G (p.Thr294Arg)
NM_001127644.2(GABRA1):c.886T>C (p.Leu296=)
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.93A>C (p.Leu31Phe)
NM_001127644.2(GABRA1):c.94C>A (p.Gln32Lys) rs769743354
NM_001127644.2(GABRA1):c.94C>T (p.Gln32Ter) rs769743354
NM_001127644.2(GABRA1):c.950T>C (p.Ile317Thr)
NM_001127644.2(GABRA1):c.954C>T (p.Ala318=) rs551045474
NM_001127644.2(GABRA1):c.962A>G (p.Tyr321Cys)
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.972G>T (p.Val324=)

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