ClinVar Miner

List of variants in gene ARSA reported as likely benign for not provided

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Gene type:
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Total variants: 18
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HGVS dbSNP
NM_000487.6(ARSA):c.1002C>T (p.Ser334=) rs147027229
NM_000487.6(ARSA):c.1149C>T (p.Asp383=) rs6151425
NM_000487.6(ARSA):c.1155C>T (p.Val385=) rs149088203
NM_000487.6(ARSA):c.1260C>T (p.Ser420=) rs1603444868
NM_000487.6(ARSA):c.222T>C (p.Ser74=) rs760597265
NM_000487.6(ARSA):c.273T>G (p.Pro91=) rs758790900
NM_000487.6(ARSA):c.279C>T (p.Val93=) rs756760904
NM_000487.6(ARSA):c.40G>A (p.Ala14Thr)
NM_000487.6(ARSA):c.466-7G>C rs6151414
NM_000487.6(ARSA):c.591C>T (p.Pro197=) rs34457249
NM_000487.6(ARSA):c.618C>T (p.Phe206=) rs370296376
NM_000487.6(ARSA):c.636C>T (p.Ala212=) rs200182983
NM_000487.6(ARSA):c.696C>T (p.Tyr232=) rs1603444965
NM_000487.6(ARSA):c.6C>T (p.Ser2=) rs1373055038
NM_000487.6(ARSA):c.720T>C (p.Phe240=) rs1603444964
NM_000487.6(ARSA):c.930C>T (p.Gly310=) rs767751622
NM_000487.6(ARSA):c.980-10C>T rs1486892120
NM_000487.6(ARSA):c.990C>T (p.His330=) rs768366772

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