List of variants in gene TYR reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1037-7T>A	rs61754381	0.00051
NM_000372.5(TYR):c.832C>T (p.Arg278Ter)	rs62645904	0.00009
NM_000372.5(TYR):c.1A>G (p.Met1Val)	rs28940881	0.00006
NM_000372.5(TYR):c.976C>T (p.Gln326Ter)	rs540911439	0.00001
NM_000372.5(TYR):c.1202T>C (p.Leu401Pro)	rs2135324201
NM_000372.5(TYR):c.1234C>G (p.Pro412Ala)	rs797046081
NM_000372.5(TYR):c.157G>C (p.Gly53Arg)	rs1591133731
NM_000372.5(TYR):c.819G>A (p.Gln273=)

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