ClinVar Miner

List of variants in gene ARSB reported as uncertain significance by Laboratory of Diagnosis and Therapy of Lysosomal Disorders,University of Padova

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Gene type:
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Total variants: 89
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HGVS dbSNP
NM_000046.4(ARSB):c.1001G>T (p.Ser334Ile) rs1554079311
NM_000046.4(ARSB):c.1028A>T (p.Lys343Met) rs1554079305
NM_000046.4(ARSB):c.1032C>G (p.Asn344Lys) rs1554079304
NM_000046.4(ARSB):c.1057T>A (p.Trp353Arg) rs1554079297
NM_000046.4(ARSB):c.1115A>G (p.Asp372Gly) rs1554079277
NM_000046.4(ARSB):c.1163G>C (p.Arg388Thr) rs1554074134
NM_000046.4(ARSB):c.1178A>C (p.His393Pro) rs118203944
NM_000046.4(ARSB):c.1178A>G (p.His393Arg) rs118203944
NM_000046.4(ARSB):c.1195T>C (p.Phe399Leu) rs762979755
NM_000046.4(ARSB):c.1213+5G>A rs1554074119
NM_000046.4(ARSB):c.1214G>A (p.Cys405Tyr) rs118203941
NM_000046.4(ARSB):c.1288C>A (p.His430Asn) rs1554069785
NM_000046.4(ARSB):c.1301G>T (p.Arg434Ile) rs1252936336
NM_000046.4(ARSB):c.1315A>G (p.Lys439Glu) rs1554069778
NM_000046.4(ARSB):c.1325C>T (p.Thr442Met) rs1057520739
NM_000046.4(ARSB):c.1334C>T (p.Pro445Leu) rs1554069775
NM_000046.4(ARSB):c.1336G>A (p.Gly446Ser) rs1554069772
NM_000046.4(ARSB):c.1336G>C (p.Gly446Arg) rs1554069772
NM_000046.4(ARSB):c.1340G>C (p.Cys447Ser) rs1465993279
NM_000046.4(ARSB):c.1340G>T (p.Cys447Phe) rs1465993279
NM_000046.4(ARSB):c.1349G>T (p.Trp450Leu) rs1554069685
NM_000046.4(ARSB):c.1442C>T (p.Pro481Leu) rs906245021
NM_000046.4(ARSB):c.1449A>T (p.Glu483Asp) rs1064793027
NM_000046.4(ARSB):c.1450A>G (p.Arg484Gly) rs201101343
NM_000046.4(ARSB):c.1457A>T (p.Asp486Val) rs1554069670
NM_000046.4(ARSB):c.1515C>T (p.Tyr505=) rs1554069663
NM_000046.4(ARSB):c.1534_1556del (p.Val512Profs) rs1310996698
NM_000046.4(ARSB):c.1562G>A (p.Cys521Tyr) rs1554069661
NM_000046.4(ARSB):c.1582_1596del (p.Val528_Trp532del) rs1554069658
NM_000046.4(ARSB):c.1592C>G (p.Pro531Arg) rs1554069659
NM_000046.4(ARSB):c.1600T>C (p.Ter534Gln) rs1554069657
NM_000046.4(ARSB):c.1601A>G (p.Ter534Trp) rs1554069655
NM_000046.4(ARSB):c.167G>A (p.Gly56Asp) rs1554032211
NM_000046.4(ARSB):c.171G>C (p.Trp57Cys) rs1554032205
NM_000046.4(ARSB):c.175G>A (p.Asp59Asn) rs1236509896
NM_000046.4(ARSB):c.194C>T (p.Ser65Phe) rs1233331806
NM_000046.4(ARSB):c.206C>T (p.Thr69Met) rs1554032175
NM_000046.4(ARSB):c.215T>A (p.Leu72Gln) rs397514441
NM_000046.4(ARSB):c.215T>C (p.Leu72Pro) rs397514441
NM_000046.4(ARSB):c.236G>A (p.Gly79Glu) rs1271212818
NM_000046.4(ARSB):c.246G>A (p.Leu82=) rs1035210606
NM_000046.4(ARSB):c.247G>T (p.Asp83Tyr) rs1247117898
NM_000046.4(ARSB):c.260C>G (p.Thr87Arg) rs1413561387
NM_000046.4(ARSB):c.264G>C (p.Gln88His) rs750947605
NM_000046.4(ARSB):c.271T>C (p.Cys91Arg) rs1554032113
NM_000046.4(ARSB):c.272G>A (p.Cys91Tyr) rs1554032112
NM_000046.4(ARSB):c.275C>A (p.Thr92Lys) rs751010538
NM_000046.4(ARSB):c.275C>T (p.Thr92Met) rs751010538
NM_000046.4(ARSB):c.277C>T (p.Pro93Ser) rs1554032104
NM_000046.4(ARSB):c.278C>T (p.Pro93Leu) rs1339096448
NM_000046.4(ARSB):c.288C>G (p.Ser96Arg) rs1554032095
NM_000046.4(ARSB):c.293T>C (p.Leu98Pro) rs1554032090
NM_000046.4(ARSB):c.305G>A (p.Arg102His) rs759356342
NM_000046.4(ARSB):c.312G>C (p.Gln104His) rs1478202079
NM_000046.4(ARSB):c.317G>A (p.Arg106His) rs150087888
NM_000046.4(ARSB):c.323G>T (p.Gly108Val) rs768802200
NM_000046.4(ARSB):c.332A>C (p.His111Pro) rs1554088096
NM_000046.4(ARSB):c.356_358del (p.Pro119_Ser120delinsArg) rs1554088087
NM_000046.4(ARSB):c.361T>C (p.Cys121Arg) rs1554088083
NM_000046.4(ARSB):c.384_386del (p.Leu129del) rs1180227844
NM_000046.4(ARSB):c.389C>T (p.Pro130Leu) rs1435155976
NM_000046.4(ARSB):c.410G>T (p.Gly137Val) rs118203938
NM_000046.4(ARSB):c.413A>G (p.Tyr138Cys) rs1554088061
NM_000046.4(ARSB):c.418A>C (p.Thr140Pro) rs1554088058
NM_000046.4(ARSB):c.426G>C (p.Met142Ile) rs1554088053
NM_000046.4(ARSB):c.436T>C (p.Trp146Arg) rs1554088037
NM_000046.4(ARSB):c.437G>C (p.Trp146Ser) rs1554088034
NM_000046.4(ARSB):c.437G>T (p.Trp146Leu) rs1554088034
NM_000046.4(ARSB):c.440A>C (p.His147Pro) rs1554088030
NM_000046.4(ARSB):c.464G>A (p.Cys155Tyr) rs1554088019
NM_000046.4(ARSB):c.489_491del (p.Thr164del) rs1214445569
NM_000046.4(ARSB):c.499G>A (p.Gly167Arg) rs1554087999
NM_000046.4(ARSB):c.523T>G (p.Tyr175Asp) rs748739839
NM_000046.4(ARSB):c.635C>T (p.Thr212Ile) rs1554087409
NM_000046.4(ARSB):c.707T>C (p.Leu236Pro) rs118203940
NM_000046.4(ARSB):c.716A>G (p.Gln239Arg) rs1554086431
NM_000046.4(ARSB):c.719C>T (p.Ser240Phe) rs1554086430
NM_000046.4(ARSB):c.725A>C (p.His242Pro) rs1554086428
NM_000046.4(ARSB):c.797A>C (p.Tyr266Ser) rs1554086402
NM_000046.4(ARSB):c.803G>T (p.Gly268Val) rs1554086400
NM_000046.4(ARSB):c.900T>A (p.Asp300Glu) rs1280123243
NM_000046.4(ARSB):c.900T>G (p.Asp300Glu) rs1280123243
NM_000046.4(ARSB):c.904G>A (p.Gly302Arg) rs779378413
NM_000046.4(ARSB):c.922G>A (p.Gly308Arg) rs1554079335
NM_000046.4(ARSB):c.923G>A (p.Gly308Glu) rs1554079333
NM_000046.4(ARSB):c.937C>T (p.Pro313Ser) rs749989641
NM_000046.4(ARSB):c.944G>C (p.Arg315Pro) rs727503809
NM_000046.4(ARSB):c.960C>G (p.Ser320Arg) rs762614315
NM_000046.5(ARSB):c.347C>A (p.Pro116His) rs775780931

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