List of variants in gene TYR reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.454C>T (p.Pro152Ser)	rs145513733	0.00024
NM_000372.5(TYR):c.1309G>A (p.Asp437Asn)	rs770006288	0.00002
NM_000372.5(TYR):c.1114G>A (p.Gly372Arg)	rs2496618651
NM_000372.5(TYR):c.308G>T (p.Cys103Phe)	rs1943252098
NM_000372.5(TYR):c.797CAT[1] (p.Ser267del)	rs2496530826

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