ClinVar Miner

List of variants in gene GABRA1 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
Download table as spreadsheet
HGVS dbSNP
NM_000806.5(GABRA1):c.-248+10C>T rs1050530276
NM_001127644.2(GABRA1):c.*2T>A rs762836110
NM_001127644.2(GABRA1):c.-15-20C>T rs555933670
NM_001127644.2(GABRA1):c.-15-23T>A rs534129599
NM_001127644.2(GABRA1):c.-15-25G>T rs200321984
NM_001127644.2(GABRA1):c.-16+18C>G rs978912528
NM_001127644.2(GABRA1):c.-16+8C>A rs138671319
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.-257T>C rs587780946
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.1059+15G>A rs2279020
NM_001127644.2(GABRA1):c.1059+8C>A rs758699164
NM_001127644.2(GABRA1):c.1060-15T>C rs773638322
NM_001127644.2(GABRA1):c.1086T>C (p.Ile362=) rs187648029
NM_001127644.2(GABRA1):c.1155C>A (p.Gly385=) rs41308303
NM_001127644.2(GABRA1):c.11G>A (p.Ser4Asn) rs796052487
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.1299C>A (p.Ile433=) rs1340729708
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.187+16G>A rs1554084016
NM_001127644.2(GABRA1):c.187G>A (p.Glu63Lys) rs1554084012
NM_001127644.2(GABRA1):c.198C>T (p.Thr66=) rs770208588
NM_001127644.2(GABRA1):c.255+12C>T rs144727170
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.441G>T (p.Arg147=) rs190024862
NM_001127644.2(GABRA1):c.442A>T (p.Ile148Phe) rs797045590
NM_001127644.2(GABRA1):c.453T>C (p.Asp151=) rs1308271547
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.501G>A (p.Pro167=) rs200750234
NM_001127644.2(GABRA1):c.559+19A>G rs1554085838
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.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.74+9A>T rs41275339
NM_001127644.2(GABRA1):c.78T>C (p.Tyr26=) rs779666888
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.846A>G (p.Arg282=) rs139467768
NM_001127644.2(GABRA1):c.857-18T>C rs78782356
NM_001127644.2(GABRA1):c.857-9del rs3214859
NM_001127644.2(GABRA1):c.857-9dup rs3214859
NM_001127644.2(GABRA1):c.85C>T (p.Pro29Ser) rs143815396
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.954C>T (p.Ala318=) rs551045474
NM_001127644.2(GABRA1):c.96A>G (p.Gln32=) rs76224028

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.