ClinVar Miner

List of variants in gene ALG14 studied for congenital myasthenic syndrome 15

Included ClinVar conditions (2):
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ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_144988.4(ALG14):c.137-18T>A rs12751061 0.07764
NM_144988.4(ALG14):c.288+11A>G rs151088933 0.00322
NM_144988.4(ALG14):c.552C>T (p.Ser184=) rs148202016 0.00059
NM_144988.4(ALG14):c.182A>G (p.Asn61Ser) rs138996965 0.00056
NM_144988.4(ALG14):c.171G>A (p.Gly57=) rs141065009 0.00045
NM_144988.4(ALG14):c.291T>C (p.Tyr97=) rs199810632 0.00044
NM_144988.4(ALG14):c.354C>T (p.Thr118=) rs372809921 0.00015
NM_144988.4(ALG14):c.420+19A>G rs145885017 0.00013
NM_144988.4(ALG14):c.532G>A (p.Val178Ile) rs373069354 0.00013
NM_144988.4(ALG14):c.220G>A (p.Asp74Asn) rs769114543 0.00011
NM_144988.4(ALG14):c.179C>G (p.Ser60Cys) rs780277809 0.00010
NM_144988.4(ALG14):c.181A>G (p.Asn61Asp) rs577399329 0.00007
NM_144988.4(ALG14):c.420+15C>G rs370637303 0.00006
NM_144988.4(ALG14):c.422T>G (p.Val141Gly) rs139005007 0.00006
NM_144988.4(ALG14):c.609A>G (p.Lys203=) rs200959923 0.00006
NM_144988.4(ALG14):c.406G>A (p.Val136Met) rs374376710 0.00005
NM_144988.4(ALG14):c.540G>A (p.Thr180=) rs767937526 0.00005
NM_144988.4(ALG14):c.140G>T (p.Gly47Val) rs139758313 0.00004
NM_144988.4(ALG14):c.310C>T (p.Arg104Ter) rs367570129 0.00004
NM_144988.4(ALG14):c.326G>A (p.Arg109Gln) rs199689080 0.00004
NM_144988.4(ALG14):c.311G>A (p.Arg104Gln) rs201781289 0.00003
NM_144988.4(ALG14):c.389T>A (p.Phe130Tyr) rs150452802 0.00003
NM_144988.4(ALG14):c.570T>A (p.His190Gln) rs770065162 0.00003
NM_144988.4(ALG14):c.641G>A (p.Arg214Gln) rs767036165 0.00002
NM_144988.4(ALG14):c.190T>C (p.Ser64Pro) rs781738381 0.00001
NM_144988.4(ALG14):c.191C>T (p.Ser64Leu) rs753195443 0.00001
NM_144988.4(ALG14):c.203A>G (p.Tyr68Cys) rs368626631 0.00001
NM_144988.4(ALG14):c.234C>A (p.Ala78=) rs753730661 0.00001
NM_144988.4(ALG14):c.245A>G (p.Asn82Ser) rs1192311417 0.00001
NM_144988.4(ALG14):c.248C>A (p.Ser83Tyr) rs767402341 0.00001
NM_144988.4(ALG14):c.263G>A (p.Arg88Gln) rs768365586 0.00001
NM_144988.4(ALG14):c.277C>G (p.Pro93Ala) rs775152763 0.00001
NM_144988.4(ALG14):c.280A>G (p.Ser94Gly) rs1360024892 0.00001
NM_144988.4(ALG14):c.288G>T (p.Met96Ile) rs143242417 0.00001
NM_144988.4(ALG14):c.313A>G (p.Ile105Val) rs746270285 0.00001
NM_144988.4(ALG14):c.328G>A (p.Glu110Lys) rs976380616 0.00001
NM_144988.4(ALG14):c.371A>C (p.His124Pro) rs1553228218 0.00001
NM_144988.4(ALG14):c.420+14T>C rs200935531 0.00001
NM_144988.4(ALG14):c.421-6T>C rs764786734 0.00001
NM_144988.4(ALG14):c.421G>A (p.Val141Met) rs946253637 0.00001
NM_144988.4(ALG14):c.423G>A (p.Val141=) rs1672547192 0.00001
NM_144988.4(ALG14):c.432C>T (p.Asn144=) rs372801574 0.00001
NM_144988.4(ALG14):c.476T>C (p.Leu159Pro) rs746850097 0.00001
NM_144988.4(ALG14):c.513C>T (p.Tyr171=) rs145148882 0.00001
NM_144988.4(ALG14):c.535G>A (p.Glu179Lys) rs957188576 0.00001
NM_144988.4(ALG14):c.539C>T (p.Thr180Met) rs750820046 0.00001
NM_144988.4(ALG14):c.546C>T (p.Ser182=) rs199846785 0.00001
NM_144988.4(ALG14):c.549G>C (p.Met183Ile) rs764533791 0.00001
NM_144988.4(ALG14):c.560T>C (p.Ile187Thr) rs775514355 0.00001
NM_144988.4(ALG14):c.600G>A (p.Pro200=) rs771908149 0.00001
NM_144988.4(ALG14):c.626C>T (p.Ser209Leu) rs754944986 0.00001
NC_000001.10:g.(?_95448632)_(95538454_?)dup
NC_000001.10:g.(?_95538299)_(95538454_?)del
NM_144988.4(ALG14):c.137-15T>C rs2525848473
NM_144988.4(ALG14):c.137-8T>C rs2525848441
NM_144988.4(ALG14):c.138T>C (p.Gly46=) rs772833545
NM_144988.4(ALG14):c.165G>A (p.Leu55=) rs768248972
NM_144988.4(ALG14):c.194C>T (p.Pro65Leu) rs730882050
NM_144988.4(ALG14):c.199C>T (p.His67Tyr) rs1557657770
NM_144988.4(ALG14):c.207C>T (p.Val69=)
NM_144988.4(ALG14):c.210T>G (p.Ile70Met) rs1006151623
NM_144988.4(ALG14):c.262C>A (p.Arg88=) rs200774756
NM_144988.4(ALG14):c.288+15C>G
NM_144988.4(ALG14):c.288+18_288+23del rs761501111
NM_144988.4(ALG14):c.288+4A>G rs2100841130
NM_144988.4(ALG14):c.288+9C>T rs2525846683
NM_144988.4(ALG14):c.289-2A>G rs1673851343
NM_144988.4(ALG14):c.289-4C>T rs767492224
NM_144988.4(ALG14):c.323G>A (p.Ser108Asn) rs1673848834
NM_144988.4(ALG14):c.337C>G (p.Gln113Glu) rs1204743597
NM_144988.4(ALG14):c.342_344del (p.Trp115del) rs1210554241
NM_144988.4(ALG14):c.393C>T (p.Pro131=) rs2100771798
NM_144988.4(ALG14):c.396A>G (p.Leu132=) rs2100771768
NM_144988.4(ALG14):c.401A>C (p.His134Pro) rs2100771746
NM_144988.4(ALG14):c.402C>A (p.His134Gln) rs2525686851
NM_144988.4(ALG14):c.420+17C>T rs2525686691
NM_144988.4(ALG14):c.420+1G>A rs2525686758
NM_144988.4(ALG14):c.420+5G>A rs1571621391
NM_144988.4(ALG14):c.420+6_420+9del rs1673843345
NM_144988.4(ALG14):c.438A>G (p.Pro146=)
NM_144988.4(ALG14):c.447T>C (p.Cys149=)
NM_144988.4(ALG14):c.451C>T (p.Pro151Ser) rs2100709244
NM_144988.4(ALG14):c.453T>A (p.Pro151=)
NM_144988.4(ALG14):c.464C>T (p.Ser155Phe) rs2100709222
NM_144988.4(ALG14):c.474C>T (p.Leu158=) rs769984980
NM_144988.4(ALG14):c.478G>A (p.Gly160Arg) rs2525552720
NM_144988.4(ALG14):c.503T>G (p.Ile168Ser) rs1431105428
NM_144988.4(ALG14):c.517G>T (p.Glu173Ter) rs2525552572
NM_144988.4(ALG14):c.529C>A (p.Arg177Ser) rs1279524858
NM_144988.4(ALG14):c.531T>G (p.Arg177=) rs202102263
NM_144988.4(ALG14):c.533T>G (p.Val178Gly) rs766184799
NM_144988.4(ALG14):c.551C>G (p.Ser184Cys) rs2100709015
NM_144988.4(ALG14):c.599C>T (p.Pro200Leu) rs1014644772
NM_144988.4(ALG14):c.619C>T (p.Pro207Ser) rs2525552113
NM_144988.4(ALG14):c.621C>T (p.Pro207=) rs2525552109
NM_144988.4(ALG14):c.633C>T (p.Tyr211=) rs1050499608

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