ClinVar Miner

List of variants in gene ALK studied for Hereditary cancer-predisposing syndrome

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Total variants: 51
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HGVS dbSNP
NM_004304.5(ALK):c.-3G>C rs1031317995
NM_004304.5(ALK):c.-5G>A rs56270786
NM_004304.5(ALK):c.1110G>A (p.Glu370=) rs138784554
NM_004304.5(ALK):c.1427T>C (p.Val476Ala) rs35093491
NM_004304.5(ALK):c.1464C>T (p.Gly488=) rs56165377
NM_004304.5(ALK):c.1500A>G (p.Gln500=) rs2293564
NM_004304.5(ALK):c.2039C>T (p.Thr680Ile) rs35228363
NM_004304.5(ALK):c.2175C>T (p.Ile725=) rs57881134
NM_004304.5(ALK):c.2478C>T (p.Tyr826=) rs142126984
NM_004304.5(ALK):c.2535T>C (p.Gly845=) rs2256740
NM_004304.5(ALK):c.2676C>T (p.Ala892=) rs138668699
NM_004304.5(ALK):c.27C>G (p.Leu9=) rs4358080
NM_004304.5(ALK):c.3035C>T (p.Thr1012Met) rs35073634
NM_004304.5(ALK):c.3036G>A (p.Thr1012=) rs2293563
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.3336G>A (p.Pro1112=) rs146074150
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.3363T>A (p.Gly1121=) rs201767904
NM_004304.5(ALK):c.3366G>A (p.Leu1122=) rs758871506
NM_004304.5(ALK):c.3375C>A (p.Gly1125=) rs3795850
NM_004304.5(ALK):c.3408C>T (p.Ser1136=) rs56146053
NM_004304.5(ALK):c.3453G>A (p.Thr1151=) rs145061595
NM_004304.5(ALK):c.3594C>T (p.Leu1198=) rs56071005
NM_004304.5(ALK):c.3599C>T (p.Ala1200Val) rs200585833
NM_004304.5(ALK):c.3600G>A (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.3600G>C (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.3610C>G (p.Leu1204Val) rs1553393864
NM_004304.5(ALK):c.3633C>A (p.Thr1211=) rs144437923
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.3645G>A (p.Pro1215=) rs775768862
NM_004304.5(ALK):c.3660C>G (p.Ser1220=) rs202010057
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
NM_004304.5(ALK):c.4203T>C (p.Tyr1401=) rs55772745
NM_004304.5(ALK):c.4338C>T (p.Thr1446=) rs56132472
NM_004304.5(ALK):c.4381A>G (p.Ile1461Val) rs1670283
NM_004304.5(ALK):c.4472A>G (p.Lys1491Arg) rs1881420
NM_004304.5(ALK):c.4587C>G (p.Asp1529Glu) rs1881421
NM_004304.5(ALK):c.4596C>T (p.Asn1532=) rs1881422
NM_004304.5(ALK):c.4671A>G (p.Leu1557=) rs1488644335
NM_004304.5(ALK):c.645T>C (p.Leu215=) rs115392387
NM_004304.5(ALK):c.702T>A (p.Pro234=) rs2246745

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