ClinVar Miner

List of variants in gene GAN reported as uncertain significance by Inherited Neuropathy Consortium

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Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP
NM_022041.3(GAN):c.1012A>T (p.Lys338Ter) rs1181977802
NM_022041.3(GAN):c.1102G>A (p.Gly368Arg) rs758756818
NM_022041.3(GAN):c.1179T>A (p.Cys393Ter) rs1597406427
NM_022041.3(GAN):c.1203G>A (p.Trp401Ter) rs1349484624
NM_022041.3(GAN):c.1237-1G>A rs1597407007
NM_022041.3(GAN):c.130C>T (p.Gln44Ter) rs1597385694
NM_022041.3(GAN):c.1312G>A (p.Val438Ile) rs1246053880
NM_022041.3(GAN):c.1343G>T (p.Trp448Leu) rs1597407111
NM_022041.3(GAN):c.1391G>A (p.Cys464Tyr) rs777535272
NM_022041.3(GAN):c.1420G>C (p.Gly474Arg) rs1435035575
NM_022041.3(GAN):c.145G>A (p.Ala49Thr) rs1597385703
NM_022041.3(GAN):c.146C>A (p.Ala49Glu) rs1597385706
NM_022041.3(GAN):c.1502+1G>T rs1555511978
NM_022041.3(GAN):c.1505G>A (p.Trp502Ter) rs1597414001
NM_022041.3(GAN):c.151G>C (p.Ala51Pro) rs750258209
NM_022041.3(GAN):c.154A>G (p.Ser52Gly) rs1597385719
NM_022041.3(GAN):c.1553_1554del (p.Phe518fs) rs1597414034
NM_022041.3(GAN):c.158C>T (p.Pro53Leu) rs1597385722
NM_022041.3(GAN):c.1633C>T (p.Arg545Cys) rs112201678
NM_022041.3(GAN):c.1634G>A (p.Arg545His) rs746486469
NM_022041.3(GAN):c.168-1G>A rs1597399963
NM_022041.3(GAN):c.1684C>G (p.Pro562Ala) rs79901179
NM_022041.3(GAN):c.1709G>A (p.Cys570Tyr) rs1597414244
NM_022041.3(GAN):c.18_19insA (p.Val7fs) rs1597385624
NM_022041.3(GAN):c.20_57del (p.Val7fs) rs1316993088
NM_022041.3(GAN):c.213T>A (p.Tyr71Ter) rs750735081
NM_022041.3(GAN):c.224T>A (p.Leu75His) rs1597399997
NM_022041.3(GAN):c.236C>T (p.Ser79Leu) rs1310137430
NM_022041.3(GAN):c.244G>T (p.Val82Phe) rs371054532
NM_022041.3(GAN):c.256A>T (p.Ile86Phe) rs1597400020
NM_022041.3(GAN):c.266A>G (p.Tyr89Cys) rs1597400024
NM_022041.3(GAN):c.282+3A>C rs1597400032
NM_022041.3(GAN):c.305T>C (p.Ile102Thr) rs1597401492
NM_022041.3(GAN):c.343_360del (p.Thr115_Leu120del) rs1597401516
NM_022041.3(GAN):c.371T>G (p.Phe124Cys) rs1597401545
NM_022041.3(GAN):c.413G>A (p.Arg138His) rs119485092
NM_022041.3(GAN):c.484C>T (p.Arg162Ter) rs1300267158
NM_022041.3(GAN):c.545T>A (p.Ile182Asn) rs1258332075
NM_022041.3(GAN):c.583G>T (p.Val195Phe) rs1432344872
NM_022041.3(GAN):c.633+1G>T rs1597401738
NM_022041.3(GAN):c.724C>T (p.Arg242Ter) rs764816887
NM_022041.3(GAN):c.732del (p.Ile244fs) rs1597402826
NM_022041.3(GAN):c.805C>T (p.Arg269Trp) rs776397915
NM_022041.3(GAN):c.877C>T (p.Arg293Ter) rs370358470
NM_022041.3(GAN):c.896A>C (p.Tyr299Ser) rs1254823893
NM_022041.3(GAN):c.896A>G (p.Tyr299Cys) rs1254823893
NM_022041.3(GAN):c.926T>G (p.Leu309Arg) rs1597403384
NM_022041.3(GAN):c.971C>T (p.Ala324Val) rs778244338
NM_022041.3(GAN):c.973G>A (p.Glu325Lys) rs1597403411
NM_022041.3(GAN):c.98A>C (p.His33Pro) rs1597385674
NM_022041.3(GAN):c.994G>A (p.Gly332Arg) rs1567494825
NM_022041.4(GAN):c.1086+1G>C rs1597405785

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