ClinVar Miner

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

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Total variants: 23
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HGVS dbSNP
NM_004304.5(ALK):c.-5G>A rs56270786
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.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.3336G>A (p.Pro1112=) rs146074150
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.3600G>C (p.Ala1200=) rs56247462
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.645T>C (p.Leu215=) rs115392387
NM_004304.5(ALK):c.702T>A (p.Pro234=) rs2246745

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