ClinVar Miner

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

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Total variants: 67
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HGVS dbSNP
NM_001127644.2(GABRA1):c.1026T>C (p.Tyr342=)
NM_001127644.2(GABRA1):c.1045G>A (p.Val349Met)
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.1079C>A (p.Pro360His)
NM_001127644.2(GABRA1):c.1104C>T (p.Tyr368=) rs771832995
NM_001127644.2(GABRA1):c.1152G>A (p.Pro384=)
NM_001127644.2(GABRA1):c.1156T>G (p.Leu386Val)
NM_001127644.2(GABRA1):c.1179A>C (p.Ala393=)
NM_001127644.2(GABRA1):c.1206C>T (p.Pro402=) rs541335259
NM_001127644.2(GABRA1):c.1218A>G (p.Pro406=)
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.1284G>A (p.Pro428=) rs74873701
NM_001127644.2(GABRA1):c.148C>T (p.Leu50=)
NM_001127644.2(GABRA1):c.150A>G (p.Leu50=) rs1006797468
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.219C>T (p.Phe73=)
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.27C>A (p.Asp9Glu) rs113886269
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.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.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.477-5T>C rs779231183
NM_001127644.2(GABRA1):c.48C>T (p.Leu16=) rs1554083720
NM_001127644.2(GABRA1):c.531C>T (p.Ala177=) rs747452052
NM_001127644.2(GABRA1):c.560-9T>C rs1581207011
NM_001127644.2(GABRA1):c.576A>G (p.Ala192=) rs1319609279
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+8C>A rs376693195
NM_001127644.2(GABRA1):c.703+8C>T
NM_001127644.2(GABRA1):c.732C>T (p.Phe244=) rs1581215256
NM_001127644.2(GABRA1):c.74+10C>T rs557887445
NM_001127644.2(GABRA1):c.753C>T (p.Gly251=)
NM_001127644.2(GABRA1):c.756C>T (p.Tyr252=) rs775895535
NM_001127644.2(GABRA1):c.78T>C (p.Tyr26=) rs779666888
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.856+8C>T rs1554087151
NM_001127644.2(GABRA1):c.857-8C>T rs752572964
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.886T>C (p.Leu296=)
NM_001127644.2(GABRA1):c.93A>C (p.Leu31Phe)
NM_001127644.2(GABRA1):c.950T>C (p.Ile317Thr)
NM_001127644.2(GABRA1):c.966C>T (p.Ala322=) rs201133616
NM_001127644.2(GABRA1):c.972G>T (p.Val324=)

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