ClinVar Miner

List of variants in gene ARSB reported as benign

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Gene type:
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Total variants: 58
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HGVS dbSNP
GRCh37/hg19 5q14.1(chr5:78106062-78111731)x1
GRCh37/hg19 5q14.1(chr5:78106062-78115511)x1
GRCh37/hg19 5q14.1(chr5:78110117-78111731)x1
GRCh37/hg19 5q14.1(chr5:78110117-78115511)x1
GRCh37/hg19 5q14.1(chr5:78110117-78150147)x1
GRCh37/hg19 5q14.1(chr5:78110117-78180736)x1
GRCh37/hg19 5q14.1(chr5:78153325-78246593)x3
GRCh37/hg19 5q14.1(chr5:78153325-78250133)x3
GRCh37/hg19 5q14.1(chr5:78280531-78280745)x4
GRCh37/hg19 5q14.1(chr5:78280531-78281153)x1
GRCh37/hg19 5q14.1(chr5:78280531-78281245)x4
GRCh37/hg19 5q14.1(chr5:78280531-78287810)x0
GRCh37/hg19 5q14.1(chr5:78280531-78292577)x1
NC_000005.9:g.78282670G>A rs163125
NM_000046.3(ARSB):c.-1178A>G rs163126
NM_000046.3(ARSB):c.-840_-839dupCA rs1255033691
NM_000046.5(ARSB):c.*1257A>C rs754567
NM_000046.5(ARSB):c.*1302G>T rs754566
NM_000046.5(ARSB):c.*1469C>T rs55710452
NM_000046.5(ARSB):c.*2022T>G rs7704939
NM_000046.5(ARSB):c.*202A>G rs73770019
NM_000046.5(ARSB):c.*2654A>G
NM_000046.5(ARSB):c.*2859T>C rs116826065
NM_000046.5(ARSB):c.*2975G>T rs3088247
NM_000046.5(ARSB):c.*3181T>G rs11750774
NM_000046.5(ARSB):c.*60G>A rs2173012
NM_000046.5(ARSB):c.1068A>T (p.Thr356=) rs16876029
NM_000046.5(ARSB):c.1072G>A (p.Val358Met) rs1065757
NM_000046.5(ARSB):c.1078C>T (p.Leu360=) rs140923667
NM_000046.5(ARSB):c.1126G>A (p.Val376Met) rs1071598
NM_000046.5(ARSB):c.113_121del (p.Gly38_Gly40del) rs550086186
NM_000046.5(ARSB):c.1142+233C>T rs10039384
NM_000046.5(ARSB):c.1143-27A>C rs25415
NM_000046.5(ARSB):c.1151G>A (p.Ser384Asn) rs25414
NM_000046.5(ARSB):c.1191G>A (p.Pro397=) rs25413
NM_000046.5(ARSB):c.1214-32T>C rs7721866
NM_000046.5(ARSB):c.1362G>A (p.Pro454=) rs35757003
NM_000046.5(ARSB):c.1373A>G (p.Asn458Ser) rs144222167
NM_000046.5(ARSB):c.1446A>G (p.Glu482=) rs35714924
NM_000046.5(ARSB):c.204C>A (p.Arg68=)
NM_000046.5(ARSB):c.313-12T>C
NM_000046.5(ARSB):c.313-26T>C rs3733895
NM_000046.5(ARSB):c.313-286del rs34055862
NM_000046.5(ARSB):c.313-77G>A rs918581
NM_000046.5(ARSB):c.313-81G>A rs918580
NM_000046.5(ARSB):c.456G>T (p.Arg152=) rs140747158
NM_000046.5(ARSB):c.499+145G>C rs61216659
NM_000046.5(ARSB):c.499+160A>G rs55882246
NM_000046.5(ARSB):c.570A>G (p.Thr190=) rs148138805
NM_000046.5(ARSB):c.690+271T>G rs7730261
NM_000046.5(ARSB):c.691-22T>C rs6870443
NM_000046.5(ARSB):c.82C>T (p.Leu28=) rs138587718
NM_000046.5(ARSB):c.899-200A>G rs180049
NM_000046.5(ARSB):c.903C>T (p.Asn301=) rs147495977
NM_000046.5(ARSB):c.972A>G (p.Gly324=) rs72762973
NM_000046.5(ARSB):c.98C>T (p.Ala33Val) rs201168448
NM_198709.3(ARSB):c.-302A>G rs163127
NM_198709.3(ARSB):c.-310-12dup rs11424557

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