ClinVar Miner

List of variants in gene GABRA1 studied for Seizures

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
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.1130C>T (p.Pro377Leu) rs751571034
NM_001127644.2(GABRA1):c.1155C>A (p.Gly385=) rs41308303
NM_001127644.2(GABRA1):c.1180A>G (p.Thr394Ala) rs1414103631
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.231C>T (p.Phe77=) rs566224462
NM_001127644.2(GABRA1):c.327A>C (p.Thr109=) rs897003492
NM_001127644.2(GABRA1):c.335G>A (p.Arg112Gln) rs587777308
NM_001127644.2(GABRA1):c.339A>T (p.Leu113Phe) rs1554085513
NM_001127644.2(GABRA1):c.384C>T (p.Phe128=) rs1219475284
NM_001127644.2(GABRA1):c.441G>T (p.Arg147=) rs190024862
NM_001127644.2(GABRA1):c.501G>A (p.Pro167=) rs200750234
NM_001127644.2(GABRA1):c.94C>A (p.Gln32Lys) rs769743354
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.