ClinVar Miner

List of variants in gene GABRA1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001127644.2(GABRA1):c.559+155A>G rs73314914 0.00605
NM_001127644.2(GABRA1):c.1059+120C>T rs181429589 0.00427
NM_001127644.2(GABRA1):c.-258T>C rs183280626 0.00026
NM_001127644.2(GABRA1):c.886T>C (p.Leu296=) rs149677108 0.00021
NM_001127644.2(GABRA1):c.74+19A>G rs370522819 0.00020
NM_001127644.2(GABRA1):c.231C>T (p.Phe77=) rs566224462 0.00015
NM_001127644.2(GABRA1):c.704-17T>G rs115043829 0.00015
NM_001127644.2(GABRA1):c.-15-25G>T rs200321984 0.00014
NM_001127644.2(GABRA1):c.85C>T (p.Pro29Ser) rs143815396 0.00013
NM_001127644.2(GABRA1):c.612C>T (p.Arg204=) rs374616425 0.00011
NM_001127644.2(GABRA1):c.*2T>A rs762836110 0.00010
NM_001127644.2(GABRA1):c.846A>G (p.Arg282=) rs139467768 0.00007
NM_001127644.2(GABRA1):c.59C>T (p.Thr20Ile) rs756553428 0.00004
NM_001127644.2(GABRA1):c.873C>T (p.Leu291=) rs777911034 0.00004
NM_001127644.2(GABRA1):c.-263A>G rs763127240 0.00003
NM_001127644.2(GABRA1):c.834T>C (p.Ser278=) rs749956729 0.00003
NM_001127644.2(GABRA1):c.1146C>T (p.Gly382=) rs79593368 0.00002
NM_001127644.2(GABRA1):c.198C>T (p.Thr66=) rs770208588 0.00002
NM_001127644.2(GABRA1):c.-15-23T>A rs534129599 0.00001
NM_001127644.2(GABRA1):c.-15-9A>T rs770530140 0.00001
NM_001127644.2(GABRA1):c.-16+18C>G rs978912528 0.00001
NM_001127644.2(GABRA1):c.-241A>T rs1402044979 0.00001
NM_001127644.2(GABRA1):c.-243A>G rs1554083390 0.00001
NM_001127644.2(GABRA1):c.-24G>C rs981975825 0.00001
NM_001127644.2(GABRA1):c.1206C>T (p.Pro402=) rs541335259 0.00001
NM_001127644.2(GABRA1):c.1299C>A (p.Ile433=) rs1340729708 0.00001
NM_001127644.2(GABRA1):c.378A>G (p.Thr126=) rs756299135 0.00001
NM_001127644.2(GABRA1):c.478C>T (p.Leu160=) rs1269683161 0.00001
NM_001127644.2(GABRA1):c.78T>C (p.Tyr26=) rs779666888 0.00001
NM_001127644.2(GABRA1):c.87G>A (p.Pro29=) rs374399356 0.00001
NM_000806.5(GABRA1):c.-248+10C>T rs1050530276
NM_001127644.2(GABRA1):c.*304del rs547262225
NM_001127644.2(GABRA1):c.-15-327G>C rs181252817
NM_001127644.2(GABRA1):c.-16+15G>A rs1581172079
NM_001127644.2(GABRA1):c.-19T>C rs1057521883
NM_001127644.2(GABRA1):c.-19_-18del rs1064794832
NM_001127644.2(GABRA1):c.-247C>T rs1043312870
NM_001127644.2(GABRA1):c.11G>A (p.Ser4Asn) rs796052487
NM_001127644.2(GABRA1):c.187+16G>A rs1554084016
NM_001127644.2(GABRA1):c.255+13T>C rs1554084940
NM_001127644.2(GABRA1):c.261T>C (p.Tyr87=) rs1057523723
NM_001127644.2(GABRA1):c.414C>T (p.Asn138=) rs1057522080
NM_001127644.2(GABRA1):c.453T>C (p.Asp151=) rs1308271547
NM_001127644.2(GABRA1):c.45C>T (p.Ile15=) rs759784427
NM_001127644.2(GABRA1):c.476+19C>T rs1057522828
NM_001127644.2(GABRA1):c.477-6C>T rs1057522459
NM_001127644.2(GABRA1):c.559+19A>G rs1554085838
NM_001127644.2(GABRA1):c.703+9G>T rs768499906
NM_001127644.2(GABRA1):c.729T>C (p.His243=) rs772218052
NM_001127644.2(GABRA1):c.75-4dup rs563768487
NM_001127644.2(GABRA1):c.856+90del rs573461878
NM_001127644.2(GABRA1):c.857-9del rs3214859
NM_001127644.2(GABRA1):c.876C>A (p.Thr292=) rs2113464345

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.