List of variants in gene TYR reported as pathogenic by Revvity Omics, Revvity

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1037-7T>A	rs61754381	0.00051
NM_000372.5(TYR):c.823G>T (p.Val275Phe)	rs104894314	0.00019
NM_000372.5(TYR):c.1467dup (p.Ala490fs)	rs61754399	0.00014
NM_000372.5(TYR):c.832C>T (p.Arg278Ter)	rs62645904	0.00009
NM_000372.5(TYR):c.230G>A (p.Arg77Gln)	rs61753185	0.00007
NM_000372.5(TYR):c.896G>A (p.Arg299His)	rs61754375	0.00007
NM_000372.5(TYR):c.715C>T (p.Arg239Trp)	rs774670098	0.00003
NM_000372.5(TYR):c.976C>T (p.Gln326Ter)	rs540911439	0.00001
NM_000372.5(TYR):c.732_733del (p.Cys244_Asp245delinsTer)	rs61754368

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