ClinVar Miner

List of variants in gene ALK reported as uncertain significance for Hereditary cancer-predisposing syndrome

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Total variants: 17
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NM_004304.5(ALK):c.-3G>C rs1031317995
NM_004304.5(ALK):c.3300C>T (p.Gly1100=) rs752819935
NM_004304.5(ALK):c.3330G>C (p.Glu1110Asp) rs140606509
NM_004304.5(ALK):c.3338G>A (p.Arg1113Gln) rs199987354
NM_004304.5(ALK):c.3358C>T (p.Arg1120Trp) rs774951734
NM_004304.5(ALK):c.3362G>A (p.Gly1121Asp) rs55760835
NM_004304.5(ALK):c.3599C>T (p.Ala1200Val) rs200585833
NM_004304.5(ALK):c.3610C>G (p.Leu1204Val) rs1553393864
NM_004304.5(ALK):c.3640C>T (p.Arg1214Cys) rs758172315
NM_004304.5(ALK):c.3641G>A (p.Arg1214His) rs750194005
NM_004304.5(ALK):c.3692G>A (p.Arg1231Gln) rs200110351
NM_004304.5(ALK):c.3743G>A (p.Arg1248Gln) rs368059424
NM_004304.5(ALK):c.3745G>T (p.Asp1249Tyr) rs1553391522
NM_004304.5(ALK):c.3839C>T (p.Ala1280Val) rs74716434
NM_004304.5(ALK):c.3888G>A (p.Met1296Ile) rs1553390763
NM_004304.5(ALK):c.4019A>G (p.Glu1340Gly) rs1469977891
NM_004304.5(ALK):c.4079G>A (p.Arg1360Gln) rs1215186876

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