ClinVar Miner

List of variants in gene ARSB reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP
NM_000046.3(ARSB):c.-1015A>G rs886060801
NM_000046.3(ARSB):c.-1058A>G rs886060802
NM_000046.3(ARSB):c.-726C>T rs116419942
NM_000046.3(ARSB):c.-848C>T rs571164401
NM_000046.3(ARSB):c.-850dupT rs574333268
NM_000046.5(ARSB):c.*1147G>A rs886060792
NM_000046.5(ARSB):c.*1169T>C rs886060791
NM_000046.5(ARSB):c.*1276C>G rs886060790
NM_000046.5(ARSB):c.*1286C>T rs886060789
NM_000046.5(ARSB):c.*1360T>A rs886060788
NM_000046.5(ARSB):c.*1372dup rs551749278
NM_000046.5(ARSB):c.*1387C>T rs555581069
NM_000046.5(ARSB):c.*1499C>G rs886060787
NM_000046.5(ARSB):c.*1513C>T rs886060786
NM_000046.5(ARSB):c.*1539dup rs886060785
NM_000046.5(ARSB):c.*1610G>A rs867100156
NM_000046.5(ARSB):c.*1729del rs369595123
NM_000046.5(ARSB):c.*1899dup rs886060784
NM_000046.5(ARSB):c.*1989C>T rs878926507
NM_000046.5(ARSB):c.*2013G>A rs113059935
NM_000046.5(ARSB):c.*2080G>A rs886060783
NM_000046.5(ARSB):c.*212A>G rs561718720
NM_000046.5(ARSB):c.*2243A>G rs145585943
NM_000046.5(ARSB):c.*2287C>T rs886060782
NM_000046.5(ARSB):c.*2543_*2545dup rs397976147
NM_000046.5(ARSB):c.*2578A>T rs548093605
NM_000046.5(ARSB):c.*2608G>A rs569254528
NM_000046.5(ARSB):c.*2637_*2639dup rs886060781
NM_000046.5(ARSB):c.*2672A>G rs886060780
NM_000046.5(ARSB):c.*2707C>T rs183918206
NM_000046.5(ARSB):c.*2708G>A rs141667208
NM_000046.5(ARSB):c.*2859T>C rs116826065
NM_000046.5(ARSB):c.*3047T>C rs560253823
NM_000046.5(ARSB):c.*3152A>G rs886060779
NM_000046.5(ARSB):c.*3163T>C rs886060778
NM_000046.5(ARSB):c.*3174T>G rs886060777
NM_000046.5(ARSB):c.*3181T>A rs11750774
NM_000046.5(ARSB):c.*608G>A rs886060796
NM_000046.5(ARSB):c.*618C>T rs757857543
NM_000046.5(ARSB):c.*619G>T rs886060795
NM_000046.5(ARSB):c.*635C>G rs534480571
NM_000046.5(ARSB):c.*793T>A rs886060794
NM_000046.5(ARSB):c.*810C>T rs777160780
NM_000046.5(ARSB):c.*990C>T rs886060793
NM_000046.5(ARSB):c.1078C>T (p.Leu360=) rs140923667
NM_000046.5(ARSB):c.1231G>A (p.Ala411Thr) rs886060797
NM_000046.5(ARSB):c.1337-3T>A rs183651028
NM_000046.5(ARSB):c.1373A>G (p.Asn458Ser) rs144222167
NM_000046.5(ARSB):c.1453C>G (p.His485Asp) rs751829762
NM_000046.5(ARSB):c.1502G>A (p.Arg501His) rs190643827
NM_000046.5(ARSB):c.1533C>T (p.Pro511=) rs528157833
NM_000046.5(ARSB):c.347C>A (p.Pro116His) rs775780931
NM_000046.5(ARSB):c.406G>A (p.Ala136Thr) rs146704780
NM_000046.5(ARSB):c.510G>C (p.Leu170=) rs768312895
NM_000046.5(ARSB):c.550A>G (p.Ile184Val) rs371812342
NM_000046.5(ARSB):c.790C>A (p.His264Asn) rs558569339
NM_000046.5(ARSB):c.82C>T (p.Leu28=) rs138587718
NM_198709.3(ARSB):c.-112G>C rs886060798
NM_198709.3(ARSB):c.-187G>A rs529476939
NM_198709.3(ARSB):c.-239T>A rs115264286
NM_198709.3(ARSB):c.-246C>T rs180784385
NM_198709.3(ARSB):c.-265G>A rs72764913
NM_198709.3(ARSB):c.-276T>C rs534158632
NM_198709.3(ARSB):c.-301G>A rs886060799
NM_198709.3(ARSB):c.-310-21G>A rs538223324
NM_198709.3(ARSB):c.-311+144T>C rs886060800
NM_198709.3(ARSB):c.-311+61A>T rs138175832

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