List of variants in gene TYR reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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.1366+4A>G	rs61754398	0.00175
NM_000372.5(TYR):c.1509G>C (p.Lys503Asn)	rs138750983	0.00047
NM_000372.5(TYR):c.1067A>T (p.Asp356Val)	rs180801021	0.00037
NM_000372.5(TYR):c.915C>A (p.Asp305Glu)	rs142170797	0.00017
NM_000372.5(TYR):c.892C>T (p.Arg298Trp)	rs200854796	0.00006
NM_000372.5(TYR):c.875C>T (p.Thr292Met)	rs61754372	0.00003
NM_000372.5(TYR):c.389A>T (p.Glu130Val)	rs966882228	0.00002
NM_000372.5(TYR):c.1343A>G (p.Asp448Gly)	rs753195354	0.00001
NM_000372.5(TYR):c.1501C>T (p.Arg501Cys)
NM_000372.5(TYR):c.1556_1557del (p.Glu519fs)	rs765024056
NM_000372.5(TYR):c.16T>A (p.Leu6Met)
NM_000372.5(TYR):c.347G>A (p.Arg116Gln)
NM_000372.5(TYR):c.485G>A (p.Gly162Glu)
NM_000372.5(TYR):c.49G>A (p.Ala17Thr)

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