List of variants in gene PEX10 reported as uncertain significance by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.275G>A (p.Arg92His)	rs375649043	0.00014
NM_002617.4(PEX10):c.760G>A (p.Gly254Ser)	rs761942658	0.00009
NM_002617.4(PEX10):c.932G>A (p.Arg311Gln)	rs724160001	0.00003
NM_002617.4(PEX10):c.979T>C (p.Ter327Arg)	rs779199089	0.00003
NM_002617.4(PEX10):c.868C>G (p.His290Asp)	rs61752094	0.00002
NM_002617.4(PEX10):c.827G>T (p.Cys276Phe)	rs1414973726	0.00001
NM_002617.4(PEX10):c.913-2A>C	rs758250423	0.00001
NM_002617.4(PEX10):c.977G>A (p.Arg326His)	rs140890506	0.00001
NM_002617.4(PEX10):c.211G>A (p.Glu71Lys)	rs1291325133
NM_002617.4(PEX10):c.233A>G (p.Gln78Arg)	rs766966222
NM_002617.4(PEX10):c.830T>C (p.Leu277Pro)	rs724160000
NM_002617.4(PEX10):c.855_857dup (p.Thr286dup)	rs1553231765
NM_002617.4(PEX10):c.876CTG[1] (p.Cys293del)	rs1438047457
NM_002617.4(PEX10):c.952_954del (p.Lys318del)	rs1553231582
NM_002617.4(PEX10):c.981A>G (p.Ter327Trp)	rs1358135448

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