List of variants in gene ALK 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_004304.5(ALK):c.310C>T (p.Pro104Ser)	rs576431612	0.00026
NM_004304.5(ALK):c.4193C>T (p.Pro1398Leu)	rs531490912	0.00014
NM_004304.5(ALK):c.1999G>A (p.Gly667Arg)	rs539763601	0.00008
NM_004304.5(ALK):c.3160G>A (p.Gly1054Ser)	rs375889530	0.00007
NM_004304.5(ALK):c.1184G>A (p.Arg395His)	rs769910087	0.00006
NM_004304.5(ALK):c.397C>T (p.Arg133Cys)	rs775940832	0.00005
NM_004304.5(ALK):c.1787T>C (p.Met596Thr)	rs754810505	0.00004
NM_004304.5(ALK):c.3251G>A (p.Arg1084His)	rs760151617	0.00004
NM_004304.5(ALK):c.4801G>A (p.Ala1601Thr)	rs376702277	0.00004
NM_004304.5(ALK):c.503T>C (p.Phe168Ser)	rs755498584	0.00004
NM_004304.5(ALK):c.1726G>T (p.Glu576Ter)	rs750740789	0.00001
NM_004304.5(ALK):c.4241G>A (p.Arg1414Lys)	rs77762612	0.00001
NM_004304.5(ALK):c.1183C>T (p.Arg395Cys)	rs779282861
NM_004304.5(ALK):c.1343T>A (p.Val448Asp)	rs1425828384
NM_004304.5(ALK):c.3178C>T (p.Arg1060Cys)	rs774836034
NM_004304.5(ALK):c.4677del (p.Ser1560fs)	rs2148137540

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