ClinVar Miner

List of variants in gene GABRA1 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000806.5(GABRA1):c.-441A>G rs11576001
NM_000806.5(GABRA1):c.1065G>A (p.Lys355=) rs1554087785
NM_000806.5(GABRA1):c.1104C>T (p.Tyr368=) rs771832995
NM_000806.5(GABRA1):c.1206C>T (p.Pro402=) rs541335259
NM_000806.5(GABRA1):c.1284G>A (p.Pro428=) rs74873701
NM_000806.5(GABRA1):c.150A>G (p.Leu50=) rs1006797468
NM_000806.5(GABRA1):c.216C>T (p.Ile72=) rs200716712
NM_000806.5(GABRA1):c.477-5T>C rs779231183
NM_000806.5(GABRA1):c.48C>T (p.Leu16=) rs1554083720
NM_000806.5(GABRA1):c.576A>G (p.Ala192=) rs1319609279
NM_000806.5(GABRA1):c.74+9A>T rs41275339
NM_000806.5(GABRA1):c.756C>T (p.Tyr252=) rs775895535
NM_000806.5(GABRA1):c.856+8C>T rs1554087151
NM_000806.5(GABRA1):c.857-8C>T rs752572964
NM_001127644.2(GABRA1):c.*1506A>C rs998754
NM_001127644.2(GABRA1):c.*1929T>C rs2290733
NM_001127644.2(GABRA1):c.*470A>G rs2290732
NM_001127644.2(GABRA1):c.-142A>G rs12658835
NM_001127644.2(GABRA1):c.-31C>T rs4608967
NM_001127644.2(GABRA1):c.1059+15G>A rs2279020
NM_001127644.2(GABRA1):c.156T>C (p.Gly52=) rs1129647

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