ClinVar Miner

List of variants in gene WARS2 reported as uncertain significance for Inborn genetic diseases

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_015836.4(WARS2):c.754C>T (p.Arg252Cys) rs149657255 0.00092
NM_015836.4(WARS2):c.938A>T (p.Lys313Met) rs145867327 0.00035
NM_015836.4(WARS2):c.348+3C>T rs200060157 0.00024
NM_015836.4(WARS2):c.791A>G (p.Tyr264Cys) rs139194636 0.00024
NM_015836.4(WARS2):c.244C>G (p.Pro82Ala) rs142739265 0.00021
NM_015836.4(WARS2):c.143A>G (p.His48Arg) rs1296437426 0.00001
NM_015836.4(WARS2):c.1054G>A (p.Glu352Lys)
NM_015836.4(WARS2):c.214A>G (p.Ser72Gly)
NM_015836.4(WARS2):c.241G>A (p.Val81Ile)
NM_015836.4(WARS2):c.265C>T (p.Arg89Trp)
NM_015836.4(WARS2):c.295CTT[1] (p.Leu100del) rs772867219
NM_015836.4(WARS2):c.313A>G (p.Asn105Asp)
NM_015836.4(WARS2):c.556A>G (p.Met186Val)
NM_015836.4(WARS2):c.694C>A (p.Pro232Thr)
NM_015836.4(WARS2):c.704T>A (p.Leu235Gln)
NM_015836.4(WARS2):c.797del (p.Pro266fs) rs746478253
NM_015836.4(WARS2):c.806G>A (p.Arg269His)
NM_015836.4(WARS2):c.877C>T (p.Arg293Cys)
NM_015836.4(WARS2):c.988C>T (p.His330Tyr)

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