List of variants in gene TYR reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1037-7T>A	rs61754381	0.00051
NM_000372.5(TYR):c.649C>T (p.Arg217Trp)	rs63159160	0.00029
NM_000372.5(TYR):c.896G>A (p.Arg299His)	rs61754375	0.00006
NM_000372.5(TYR):c.1147G>A (p.Asp383Asn)	rs121908011	0.00004
NM_000372.5(TYR):c.1204C>T (p.Arg402Ter)	rs62645917	0.00004
NM_000372.5(TYR):c.832C>T (p.Arg278Ter)	rs62645904	0.00004
NM_000372.5(TYR):c.1255G>A (p.Gly419Arg)	rs61754392	0.00001
NM_000372.5(TYR):c.1037-18T>G	rs781052288
NM_000372.5(TYR):c.1037G>A (p.Gly346Glu)	rs773970123
NM_000372.5(TYR):c.1184+2T>C	rs758119014
NM_000372.5(TYR):c.164G>C (p.Cys55Ser)	rs28940879
NM_000372.5(TYR):c.223G>T (p.Asp75Tyr)	rs1565386425
NM_000372.5(TYR):c.585G>A (p.Trp195Ter)	rs147574809
NM_000372.5(TYR):c.943_948del (p.Ser315_Ala316del)	rs1565391977

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