ClinVar Miner

List of variants studied for Peroxisome biogenesis disorder, complementation group 7

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Total variants: 7
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HGVS dbSNP
NM_153818.1(PEX10):c.338del (p.Leu113fs) rs878853044
NM_153818.1(PEX10):c.600+1G>A rs267608183
NM_153818.1(PEX10):c.665G>A (p.Arg222His) rs371979619
NM_153818.1(PEX10):c.764dup (p.Leu256fs) rs61750435
NM_153818.1(PEX10):c.874_875del (p.Leu292fs) rs61752093
NM_153818.1(PEX10):c.880A>G (p.Thr294Ala) rs34154371
NM_153818.1(PEX10):c.899G>A (p.Arg300His) rs758678654

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