ClinVar Miner

List of variants in gene ALG6 studied for congenital disorder of glycosylation type I

Included ClinVar conditions (31):
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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NC_000001.10:g.(?_63862174)_(63862278_?)del
NM_013339.4(ALG6):c.1092T>C (p.Phe364=) rs751867296
NM_013339.4(ALG6):c.1127+1G>A rs1557597486
NM_013339.4(ALG6):c.1128-2A>C rs1553156882
NM_013339.4(ALG6):c.1135C>T (p.Pro379Ser) rs150976885
NM_013339.4(ALG6):c.1136del (p.Pro379fs) rs1553156884
NM_013339.4(ALG6):c.1167del (p.Ser390fs) rs769698652
NM_013339.4(ALG6):c.1193_1198del (p.Phe398_Ala400delinsSer) rs1553156893
NM_013339.4(ALG6):c.1194_1195delinsG (p.Phe398fs) rs1553156894
NM_013339.4(ALG6):c.1194dup (p.Ile399fs) rs1207096732
NM_013339.4(ALG6):c.1237_1239GAA[2] (p.Glu415del) rs773295759
NM_013339.4(ALG6):c.1357C>G (p.Leu453Val) rs41285372
NM_013339.4(ALG6):c.1364_1366TGA[1] (p.Met456del) rs1553157427
NM_013339.4(ALG6):c.1387_1388del (p.Pro463fs) rs774242915
NM_013339.4(ALG6):c.1390C>T (p.Gln464Ter) rs1553157428
NM_013339.4(ALG6):c.1394_1398dup (p.Pro467fs) rs1553157429
NM_013339.4(ALG6):c.1432T>C (p.Ser478Pro) rs121908444
NM_013339.4(ALG6):c.1469_1474del (p.Asn490_Ile491del) rs1553157450
NM_013339.4(ALG6):c.146_147del (p.Thr48_Phe49insTer)
NM_013339.4(ALG6):c.1473_1475TAT[4] (p.Ile493dup) rs1475726598
NM_013339.4(ALG6):c.1524del (p.Ter508TyrextTer?) rs759636698
NM_013339.4(ALG6):c.156G>A (p.Pro52=) rs751004049
NM_013339.4(ALG6):c.167+5G>A rs1557585860
NM_013339.4(ALG6):c.171T>A (p.Tyr57Ter) rs780528545
NM_013339.4(ALG6):c.189_191del (p.Asn64del) rs1553155267
NM_013339.4(ALG6):c.1A>G (p.Met1Val) rs562934427
NM_013339.4(ALG6):c.235_237del (p.His79del) rs1297610094
NM_013339.4(ALG6):c.250G>A (p.Ala84Thr) rs762643273
NM_013339.4(ALG6):c.257+2dup rs745426479
NM_013339.4(ALG6):c.257+5G>A rs199682486
NM_013339.4(ALG6):c.2T>C (p.Met1Thr) rs1387214955
NM_013339.4(ALG6):c.338G>A (p.Arg113His) rs768372697
NM_013339.4(ALG6):c.391T>C (p.Tyr131His) rs35383149
NM_013339.4(ALG6):c.429+1G>T rs781097055
NM_013339.4(ALG6):c.430-2A>G rs1553155565
NM_013339.4(ALG6):c.471_476del (p.156_157LI[1]) rs1553155569
NM_013339.4(ALG6):c.482A>G (p.Tyr161Cys) rs201354339
NM_013339.4(ALG6):c.495-2A>G rs1227131990
NM_013339.4(ALG6):c.495A>G (p.Gln165=) rs886046471
NM_013339.4(ALG6):c.52C>T (p.Arg18Ter) rs755933716
NM_013339.4(ALG6):c.53G>A (p.Arg18Gln) rs1287725303
NM_013339.4(ALG6):c.65_66insAAGA (p.Leu23fs) rs1553153399
NM_013339.4(ALG6):c.671A>G (p.Lys224Arg)
NM_013339.4(ALG6):c.680+2T>G
NM_013339.4(ALG6):c.680G>A (p.Gly227Glu) rs372079206
NM_013339.4(ALG6):c.726C>T (p.Phe242=) rs59848367
NM_013339.4(ALG6):c.732_748dup (p.Phe250fs) rs1553155823
NM_013339.4(ALG6):c.751A>G (p.Thr251Ala) rs61755863
NM_013339.4(ALG6):c.781_783AGA[1] (p.Arg262del) rs886548508
NM_013339.4(ALG6):c.82_82+8del rs1424742651
NM_013339.4(ALG6):c.894_896AAT[1] (p.Ile299del) rs387906338
NM_013339.4(ALG6):c.902+1G>A
NM_013339.4(ALG6):c.988G>T (p.Val330Phe) rs1057518724
NM_013339.4(ALG6):c.998C>T (p.Ala333Val) rs121908443
NM_013339.4(ALG6):c.999dup (p.Leu334fs)

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