ClinVar Miner

List of variants in gene ALK reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_004304.5(ALK):c.*111C>T rs74669215
NM_004304.5(ALK):c.*298C>T rs1728828
NM_004304.5(ALK):c.*45G>A rs186421480
NM_004304.5(ALK):c.*53G>C rs80088378
NM_004304.5(ALK):c.*61_*64dup rs397706189
NM_004304.5(ALK):c.*63A>G rs182561050
NM_004304.5(ALK):c.-539G>A
NM_004304.5(ALK):c.1111G>A (p.Ala371Thr) rs149968229
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.1720G>C (p.Gly574Arg)
NM_004304.5(ALK):c.2011C>T (p.Pro671Ser) rs145780832
NM_004304.5(ALK):c.2039C>T (p.Thr680Ile) rs35228363
NM_004304.5(ALK):c.2127C>A (p.Asn709Lys) rs376175333
NM_004304.5(ALK):c.2133C>T (p.Ser711=) rs77102810
NM_004304.5(ALK):c.2148C>T (p.Ser716=) rs55733526
NM_004304.5(ALK):c.2175C>T (p.Ile725=) rs57881134
NM_004304.5(ALK):c.2430C>T (p.Ser810=) rs150292405
NM_004304.5(ALK):c.2478C>T (p.Tyr826=) rs142126984
NM_004304.5(ALK):c.2526C>T (p.Ala842=) rs145271283
NM_004304.5(ALK):c.2535T>C (p.Gly845=) rs2256740
NM_004304.5(ALK):c.2613C>T (p.Asn871=) rs150557024
NM_004304.5(ALK):c.2676C>T (p.Ala892=) rs138668699
NM_004304.5(ALK):c.2775A>G (p.Gly925=)
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.3057C>A (p.Val1019=) rs138406372
NM_004304.5(ALK):c.3291C>T (p.Cys1097=) rs370170353
NM_004304.5(ALK):c.3336G>A (p.Pro1112=) rs146074150
NM_004304.5(ALK):c.3359+6C>T rs4622670
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.3594C>T (p.Leu1198=) rs56071005
NM_004304.5(ALK):c.3600G>C (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.3939-8A>G rs3738869
NM_004304.5(ALK):c.4165-6C>T rs17007646
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.4480G>A (p.Gly1494Arg) rs199940609
NM_004304.5(ALK):c.4573A>G (p.Lys1525Glu) rs139437088
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.4836G>A (p.Lys1612=) rs78174819
NM_004304.5(ALK):c.487G>T (p.Val163Leu) rs55697431
NM_004304.5(ALK):c.645T>C (p.Leu215=) rs115392387
NM_004304.5(ALK):c.702T>A (p.Pro234=) rs2246745

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