ClinVar Miner

List of variants in gene GABRA1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NM_000806.5(GABRA1):c.-248+5C>T
NM_000806.5(GABRA1):c.-248+8C>A rs886060358
NM_000806.5(GABRA1):c.-399C>T
NM_000806.5(GABRA1):c.-405T>C rs181962869
NM_000806.5(GABRA1):c.-438del rs112361424
NM_000806.5(GABRA1):c.-439A>G rs886060357
NM_000806.5(GABRA1):c.-442dup rs201310567
NM_000806.5(GABRA1):c.-447G>C
NM_000806.5(GABRA1):c.-447G>T
NM_000806.5(GABRA1):c.-448G>A rs11576000
NM_000806.5(GABRA1):c.-448G>C rs11576000
NM_000806.5(GABRA1):c.-449G>C rs190043578
NM_000806.5(GABRA1):c.-455G>A rs531705924
NM_001127644.2(GABRA1):c.*1061T>C rs374002978
NM_001127644.2(GABRA1):c.*1319A>G rs886060367
NM_001127644.2(GABRA1):c.*1324T>C
NM_001127644.2(GABRA1):c.*1359T>C
NM_001127644.2(GABRA1):c.*1381T>C rs187522588
NM_001127644.2(GABRA1):c.*1425T>C
NM_001127644.2(GABRA1):c.*1426A>G
NM_001127644.2(GABRA1):c.*1443A>G rs575959204
NM_001127644.2(GABRA1):c.*1512G>A rs886060368
NM_001127644.2(GABRA1):c.*1526A>G rs540638714
NM_001127644.2(GABRA1):c.*1601T>G rs886060369
NM_001127644.2(GABRA1):c.*1609A>C
NM_001127644.2(GABRA1):c.*1611G>A
NM_001127644.2(GABRA1):c.*1659A>G rs886060370
NM_001127644.2(GABRA1):c.*1685C>T
NM_001127644.2(GABRA1):c.*1686G>A
NM_001127644.2(GABRA1):c.*1697A>G
NM_001127644.2(GABRA1):c.*1749T>C
NM_001127644.2(GABRA1):c.*1752G>T rs41303356
NM_001127644.2(GABRA1):c.*1781T>C
NM_001127644.2(GABRA1):c.*1821T>G rs10059108
NM_001127644.2(GABRA1):c.*1837C>G rs886060371
NM_001127644.2(GABRA1):c.*1938A>G
NM_001127644.2(GABRA1):c.*1971T>C rs886060372
NM_001127644.2(GABRA1):c.*1984T>C
NM_001127644.2(GABRA1):c.*2009G>C
NM_001127644.2(GABRA1):c.*2035G>A
NM_001127644.2(GABRA1):c.*2098C>T
NM_001127644.2(GABRA1):c.*213C>T rs886060362
NM_001127644.2(GABRA1):c.*2279G>A rs575186628
NM_001127644.2(GABRA1):c.*2334C>T rs886060373
NM_001127644.2(GABRA1):c.*242C>G
NM_001127644.2(GABRA1):c.*2523A>C rs567624810
NM_001127644.2(GABRA1):c.*302A>G rs886060364
NM_001127644.2(GABRA1):c.*304del rs547262225
NM_001127644.2(GABRA1):c.*325T>A
NM_001127644.2(GABRA1):c.*398A>C rs374845401
NM_001127644.2(GABRA1):c.*401G>A rs541504060
NM_001127644.2(GABRA1):c.*413G>A rs886060365
NM_001127644.2(GABRA1):c.*433G>C
NM_001127644.2(GABRA1):c.*438A>C
NM_001127644.2(GABRA1):c.*456C>T
NM_001127644.2(GABRA1):c.*580G>A
NM_001127644.2(GABRA1):c.*580G>T
NM_001127644.2(GABRA1):c.*630T>C
NM_001127644.2(GABRA1):c.*771C>T rs886060366
NM_001127644.2(GABRA1):c.*826G>A
NM_001127644.2(GABRA1):c.*838G>A
NM_001127644.2(GABRA1):c.*988A>G
NM_001127644.2(GABRA1):c.*993C>T
NM_001127644.2(GABRA1):c.-10C>G rs376699435
NM_001127644.2(GABRA1):c.-117_-112GACTCG[3] rs527890421
NM_001127644.2(GABRA1):c.-15-5T>G
NM_001127644.2(GABRA1):c.-16+8C>A rs138671319
NM_001127644.2(GABRA1):c.-162G>A
NM_001127644.2(GABRA1):c.-195A>G rs886060359
NM_001127644.2(GABRA1):c.-220T>C rs186477194
NM_001127644.2(GABRA1):c.-252T>C rs766490931
NM_001127644.2(GABRA1):c.-4C>T rs375475234
NM_001127644.2(GABRA1):c.1079C>A (p.Pro360His)
NM_001127644.2(GABRA1):c.1155C>A (p.Gly385=) rs41308303
NM_001127644.2(GABRA1):c.1206C>T (p.Pro402=) rs541335259
NM_001127644.2(GABRA1):c.1290A>G (p.Leu430=) rs886060361
NM_001127644.2(GABRA1):c.1322C>T (p.Thr441Met)
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.191G>A (p.Arg64His)
NM_001127644.2(GABRA1):c.234A>C (p.Gly78=)
NM_001127644.2(GABRA1):c.243A>C (p.Ser81=)
NM_001127644.2(GABRA1):c.255+12C>T rs144727170
NM_001127644.2(GABRA1):c.477-14A>G rs757378039
NM_001127644.2(GABRA1):c.501G>A (p.Pro167=) rs200750234
NM_001127644.2(GABRA1):c.672A>G (p.Thr224=) rs372742479
NM_001127644.2(GABRA1):c.703+8C>A rs376693195
NM_001127644.2(GABRA1):c.856+11A>G rs564871157
NM_001127644.2(GABRA1):c.857-5T>C rs543710675
NM_001127644.2(GABRA1):c.93A>C (p.Leu31Phe)
NM_001127644.2(GABRA1):c.954C>T (p.Ala318=) rs551045474
NM_001127644.2(GABRA1):c.96A>G (p.Gln32=) rs76224028

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