ClinVar Miner

List of variants in gene RARS1 reported as uncertain significance by GeneDx

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_002887.4(RARS1):c.206C>T (p.Pro69Leu) rs34446466 0.00049
NM_002887.4(RARS1):c.220A>G (p.Ile74Val) rs144947867 0.00037
NM_002887.4(RARS1):c.208A>G (p.Thr70Ala) rs576527619 0.00033
NM_002887.4(RARS1):c.1465G>A (p.Glu489Lys) rs11557638 0.00022
NM_002887.4(RARS1):c.1903A>T (p.Met635Leu) rs150166808 0.00019
NM_002887.4(RARS1):c.668G>A (p.Arg223His) rs146632182 0.00011
NM_002887.4(RARS1):c.1568T>A (p.Met523Lys) rs1064796563 0.00001
NM_002887.4(RARS1):c.23G>T (p.Cys8Phe) rs779497127 0.00001
NM_002887.4(RARS1):c.-5G>A
NM_002887.4(RARS1):c.17C>T (p.Ser6Phe)
NM_002887.4(RARS1):c.1820C>T (p.Ala607Val)
NM_002887.4(RARS1):c.19G>C (p.Glu7Gln)
NM_002887.4(RARS1):c.227TTA[1] (p.Ile77del)
NM_002887.4(RARS1):c.305T>A (p.Val102Glu)
NM_002887.4(RARS1):c.361A>G (p.Ile121Val)
NM_002887.4(RARS1):c.365C>T (p.Ser122Phe)
NM_002887.4(RARS1):c.653G>C (p.Gly218Ala)
NM_002887.4(RARS1):c.741G>A (p.Met247Ile)
NM_002887.4(RARS1):c.825dup (p.Ser276fs) rs780133021

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