List of variants in gene TET3 reported as pathogenic for Beck-Fahrner syndrome

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001287491.2(TET3):c.2254C>T (p.Arg752Cys)	rs534089911	0.00008
NM_001287491.2(TET3):c.1215del (p.Trp406fs)	rs1573779765
NM_001287491.2(TET3):c.1349G>A (p.Trp450Ter)
NM_001287491.2(TET3):c.2161_2183dup (p.Ser729fs)	rs2103698244
NM_001287491.2(TET3):c.2552C>T (p.Thr851Met)	rs1573856970
NM_001287491.2(TET3):c.2722G>T (p.Val908Leu)	rs1227643933
NM_001287491.2(TET3):c.3215T>G (p.Phe1072Cys)	rs1573906351
NM_001287491.2(TET3):c.3226G>A (p.Ala1076Thr)	rs1573906389
NM_001287491.2(TET3):c.3265G>A (p.Val1089Met)	rs1174857008
NM_001287491.2(TET3):c.3448C>T (p.Arg1150Ter)
NM_001287491.2(TET3):c.4977_4983del (p.His1660fs)	rs1572907400
NM_001287491.2(TET3):c.5083C>T (p.Gln1695Ter)	rs1572907595

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