ClinVar Miner

List of variants in gene GABRG2 reported as uncertain significance by Invitae

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Gene type:
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Total variants: 83
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HGVS dbSNP
NC_000005.9:g.(?_161528235)_(161580379_?)dup
NC_000005.9:g.(?_161528241)_(161582545_?)dup
NM_198903.2(GABRG2):c.1027G>A (p.Ala343Thr) rs1581439874
NM_198903.2(GABRG2):c.1047C>G (p.Ile349Met) rs1554100910
NM_198903.2(GABRG2):c.106G>A (p.Gly36Ser) rs866056788
NM_198903.2(GABRG2):c.1072C>G (p.Leu358Val) rs1561660795
NM_198903.2(GABRG2):c.1094C>T (p.Ser365Leu) rs1581453572
NM_198903.2(GABRG2):c.1105G>T (p.Val369Phe) rs768061156
NM_198903.2(GABRG2):c.1120G>A (p.Ala374Thr) rs398123523
NM_198903.2(GABRG2):c.1127A>G (p.Asp376Gly) rs1060501890
NM_198903.2(GABRG2):c.11C>T (p.Pro4Leu) rs375295110
NM_198903.2(GABRG2):c.1207C>T (p.Arg403Trp) rs374512652
NM_198903.2(GABRG2):c.1208G>A (p.Arg403Gln) rs780199000
NM_198903.2(GABRG2):c.1233_1235del (p.Lys414del) rs727503941
NM_198903.2(GABRG2):c.1273-2A>G rs1554101185
NM_198903.2(GABRG2):c.1276C>T (p.Pro426Ser) rs757311213
NM_198903.2(GABRG2):c.1292G>A (p.Arg431His) rs528036202
NM_198903.2(GABRG2):c.1317G>T (p.Met439Ile) rs1581462722
NM_198903.2(GABRG2):c.1399T>C (p.Cys467Arg) rs1200142311
NM_198903.2(GABRG2):c.1418G>A (p.Arg473Gln) rs774474550
NM_198903.2(GABRG2):c.1454G>T (p.Arg485Leu) rs587780341
NM_198903.2(GABRG2):c.1480C>T (p.Arg494Trp) rs796052515
NM_198903.2(GABRG2):c.1513A>T (p.Asn505Tyr) rs1581463309
NM_198903.2(GABRG2):c.1535dup (p.Tyr512Ter) rs1210628894
NM_198903.2(GABRG2):c.173C>A (p.Thr58Asn) rs763218917
NM_198903.2(GABRG2):c.17T>C (p.Ile6Thr) rs759392289
NM_198903.2(GABRG2):c.191G>A (p.Gly64Asp) rs1408343754
NM_198903.2(GABRG2):c.353C>T (p.Ala118Val) rs772800839
NM_198903.2(GABRG2):c.365A>G (p.Tyr122Cys) rs1554097875
NM_198903.2(GABRG2):c.37G>A (p.Val13Ile) rs796052502
NM_198903.2(GABRG2):c.455T>C (p.Phe152Ser) rs1581350948
NM_198903.2(GABRG2):c.470A>C (p.Lys157Thr) rs770364855
NM_198903.2(GABRG2):c.530G>A (p.Arg177Gln) rs1445637165
NM_198903.2(GABRG2):c.549-3T>G rs750459631
NM_198903.2(GABRG2):c.579A>G (p.Gln193=) rs751723547
NM_198903.2(GABRG2):c.583C>A (p.His195Asn) rs981863613
NM_198903.2(GABRG2):c.596T>C (p.Met199Thr) rs770506471
NM_198903.2(GABRG2):c.608C>G (p.Ser203Cys) rs1334273668
NM_198903.2(GABRG2):c.71C>A (p.Thr24Lys) rs1060501891
NM_198903.2(GABRG2):c.764G>C (p.Arg255Pro) rs1561645172
NM_198903.2(GABRG2):c.764G>T (p.Arg255Leu) rs1561645172
NM_198903.2(GABRG2):c.811G>A (p.Asp271Asn) rs773065895
NM_198903.2(GABRG2):c.868G>A (p.Glu290Lys) rs549251133
NM_198903.2(GABRG2):c.958T>G (p.Tyr320Asp) rs1581439671
NM_198904.4(GABRG2):c.1001C>T (p.Ala334Val)
NM_198904.4(GABRG2):c.1010T>G (p.Leu337Arg)
NM_198904.4(GABRG2):c.1012T>C (p.Phe338Leu)
NM_198904.4(GABRG2):c.1045G>A (p.Ala349Thr)
NM_198904.4(GABRG2):c.1053G>A (p.Val351=)
NM_198904.4(GABRG2):c.1108G>T (p.Asp370Tyr)
NM_198904.4(GABRG2):c.1115A>G (p.Lys372Arg)
NM_198904.4(GABRG2):c.1179A>T (p.Arg393Ser)
NM_198904.4(GABRG2):c.1189A>G (p.Ile397Val)
NM_198904.4(GABRG2):c.1208C>T (p.Thr403Ile)
NM_198904.4(GABRG2):c.126TGA[2] (p.Asp45del)
NM_198904.4(GABRG2):c.1331T>C (p.Ile444Thr)
NM_198904.4(GABRG2):c.1383C>G (p.Phe461Leu)
NM_198904.4(GABRG2):c.248C>T (p.Pro83Leu)
NM_198904.4(GABRG2):c.372A>T (p.Arg124Ser)
NM_198904.4(GABRG2):c.389G>A (p.Ser130Asn)
NM_198904.4(GABRG2):c.394A>G (p.Ile132Val)
NM_198904.4(GABRG2):c.394A>T (p.Ile132Phe)
NM_198904.4(GABRG2):c.403C>T (p.Leu135Phe)
NM_198904.4(GABRG2):c.432A>C (p.Lys144Asn)
NM_198904.4(GABRG2):c.447C>A (p.Asp149Glu)
NM_198904.4(GABRG2):c.49C>G (p.Pro17Ala)
NM_198904.4(GABRG2):c.549G>A (p.Arg183=)
NM_198904.4(GABRG2):c.631+4A>C
NM_198904.4(GABRG2):c.631+6T>C
NM_198904.4(GABRG2):c.632-10C>A
NM_198904.4(GABRG2):c.643C>T (p.Arg215Cys)
NM_198904.4(GABRG2):c.644G>A (p.Arg215His)
NM_198904.4(GABRG2):c.650A>G (p.Glu217Gly)
NM_198904.4(GABRG2):c.727G>T (p.Val243Phe)
NM_198904.4(GABRG2):c.761C>T (p.Thr254Ile)
NM_198904.4(GABRG2):c.769+5G>C
NM_198904.4(GABRG2):c.859G>A (p.Val287Ile)
NM_198904.4(GABRG2):c.872G>C (p.Trp291Ser)
NM_198904.4(GABRG2):c.890A>G (p.Asn297Ser)
NM_198904.4(GABRG2):c.893A>C (p.Lys298Thr)
NM_198904.4(GABRG2):c.950C>G (p.Thr317Ser)
NM_198904.4(GABRG2):c.965C>A (p.Ala322Asp)
NM_198904.4(GABRG2):c.967C>G (p.Arg323Gly)

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