ClinVar Miner

List of variants in gene PEX10 reported as uncertain significance for Peroxisome biogenesis disorder 6A; Peroxisome biogenesis disorder 6B

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Gene type:
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Total variants: 16
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NM_002617.3(PEX10):c.855_857dup (p.Thr286dup) rs1553231765
NM_002617.3(PEX10):c.876_878CTG[1] (p.Cys293del) rs1438047457
NM_002617.3(PEX10):c.952_954del (p.Lys318del) rs1553231582
NM_153818.1(PEX10):c.1037G>A (p.Arg346His) rs140890506
NM_153818.1(PEX10):c.1039T>C (p.Ter347Arg) rs779199089
NM_153818.1(PEX10):c.1041A>G (p.Ter347Trp) rs1358135448
NM_153818.1(PEX10):c.211G>A (p.Glu71Lys) rs1291325133
NM_153818.1(PEX10):c.233A>G (p.Gln78Arg) rs766966222
NM_153818.1(PEX10):c.275G>A (p.Arg92His) rs375649043
NM_153818.1(PEX10):c.772G>C (p.Gly258Arg) rs61736380
NM_153818.1(PEX10):c.820G>A (p.Gly274Ser) rs761942658
NM_153818.1(PEX10):c.887G>T (p.Cys296Phe) rs1414973726
NM_153818.1(PEX10):c.890T>C (p.Leu297Pro) rs724160000
NM_153818.1(PEX10):c.928C>G (p.His310Asp) rs61752094
NM_153818.1(PEX10):c.973-2A>C rs758250423
NM_153818.1(PEX10):c.992G>A (p.Arg331Gln) rs724160001

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