ClinVar Miner

List of variants in gene ARSA reported as uncertain significance for not provided

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Total variants: 27
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HGVS dbSNP
NM_000487.6(ARSA):c.1115G>C (p.Arg372Pro) rs74315477
NM_000487.6(ARSA):c.1174C>T (p.Arg392Trp) rs74315480
NM_000487.6(ARSA):c.1178C>G (p.Thr393Ser) rs743616
NM_000487.6(ARSA):c.1211-10C>T rs398123413
NM_000487.6(ARSA):c.1334G>T (p.Gly445Val) rs540762357
NM_000487.6(ARSA):c.1447G>A (p.Glu483Lys) rs148352371
NM_000487.6(ARSA):c.1471T>C (p.Cys491Arg) rs199476388
NM_000487.6(ARSA):c.225-5C>G rs192013394
NM_000487.6(ARSA):c.325G>A (p.Val109Met) rs746259972
NM_000487.6(ARSA):c.329C>T (p.Ala110Val) rs1191014984
NM_000487.6(ARSA):c.369_374delinsAACCTTGGG (p.Gly124_Lys125delinsThrLeuGly) rs786200965
NM_000487.6(ARSA):c.370G>A (p.Gly124Ser) rs74315461
NM_000487.6(ARSA):c.465G>A (p.Gln155=) rs199476377
NM_000487.6(ARSA):c.466-7G>C rs6151414
NM_000487.6(ARSA):c.632T>C (p.Met211Thr)
NM_000487.6(ARSA):c.640G>A (p.Ala214Thr) rs199476341
NM_000487.6(ARSA):c.656G>A (p.Arg219His) rs148403406
NM_000487.6(ARSA):c.677C>T (p.Ala226Val) rs74315468
NM_000487.6(ARSA):c.685-7C>A rs398123417
NM_000487.6(ARSA):c.799A>G (p.Ile267Val)
NM_000487.6(ARSA):c.847G>T (p.Asp283Tyr) rs199476386
NM_000487.6(ARSA):c.854+3A>G rs1057524566
NM_000487.6(ARSA):c.854+5G>T rs886043370
NM_000487.6(ARSA):c.901C>G (p.Arg301Gly) rs794727704
NM_000487.6(ARSA):c.918G>A (p.Thr306=) rs370250328
NM_000487.6(ARSA):c.930C>T (p.Gly310=) rs767751622
NM_000487.6(ARSA):c.932G>A (p.Gly311Asp) rs886042812

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