ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_004304.5(ALK):c.*298C>T rs1728828 0.99040
NM_004304.5(ALK):c.4381A>G (p.Ile1461Val) rs1670283 0.99030
NM_004304.5(ALK):c.27C>G (p.Leu9=) rs4358080 0.88526
NM_004304.5(ALK):c.1500A>G (p.Gln500=) rs2293564 0.79300
NM_004304.5(ALK):c.2535T>C (p.Gly845=) rs2256740 0.63034
NM_004304.5(ALK):c.4587C>G (p.Asp1529Glu) rs1881421 0.47503
NM_004304.5(ALK):c.3375C>A (p.Gly1125=) rs3795850 0.27292
NM_004304.5(ALK):c.4472A>G (p.Lys1491Arg) rs1881420 0.26767
NM_004304.5(ALK):c.*61_*64dup rs397706189 0.25265
NM_004304.5(ALK):c.3359+6C>T rs4622670 0.24182
NM_004304.5(ALK):c.4165-6C>T rs17007646 0.20768
NM_004304.5(ALK):c.3036G>A (p.Thr1012=) rs2293563 0.17851
NM_004304.5(ALK):c.4338C>T (p.Thr1446=) rs56132472 0.10831
NM_004304.5(ALK):c.3408C>T (p.Ser1136=) rs56146053 0.02769
NM_004304.5(ALK):c.*53G>C rs80088378 0.02692
NM_004304.5(ALK):c.1427T>C (p.Val476Ala) rs35093491 0.02566
NM_004304.5(ALK):c.4596C>T (p.Asn1532=) rs1881422 0.01874
NM_004304.5(ALK):c.4203T>C (p.Tyr1401=) rs55772745 0.01865
NM_004304.5(ALK):c.*111C>T rs74669215 0.01748
NM_004304.5(ALK):c.*63A>G rs182561050 0.01679
NM_004304.5(ALK):c.2039C>T (p.Thr680Ile) rs35228363 0.01598
NM_004304.5(ALK):c.645T>C (p.Leu215=) rs115392387 0.00889
NM_004304.5(ALK):c.2175C>T (p.Ile725=) rs57881134 0.00677
NM_004304.5(ALK):c.2133C>T (p.Ser711=) rs77102810 0.00647
NM_004304.5(ALK):c.1464C>T (p.Gly488=) rs56165377 0.00615
NM_004304.5(ALK):c.4836G>A (p.Lys1612=) rs78174819 0.00363
NM_004304.5(ALK):c.3594C>T (p.Leu1198=) rs56071005 0.00166
NM_004304.5(ALK):c.2676C>T (p.Ala892=) rs138668699 0.00164
NM_004304.5(ALK):c.2148C>T (p.Ser716=) rs55733526 0.00096
NM_004304.5(ALK):c.2613C>T (p.Asn871=) rs150557024 0.00093
NM_004304.5(ALK):c.2430C>T (p.Ser810=) rs150292405 0.00086
NM_004304.5(ALK):c.3939-8A>G rs3738869 0.00054
NM_004304.5(ALK):c.3057C>A (p.Val1019=) rs138406372 0.00043
NM_004304.5(ALK):c.2526C>T (p.Ala842=) rs145271283 0.00029
NM_004304.5(ALK):c.4573A>G (p.Lys1525Glu) rs139437088 0.00024
NM_004304.5(ALK):c.3291C>T (p.Cys1097=) rs370170353 0.00022
NM_004304.5(ALK):c.3035C>T (p.Thr1012Met) rs35073634 0.00021
NM_004304.5(ALK):c.3336G>A (p.Pro1112=) rs146074150 0.00019
NM_004304.5(ALK):c.487G>T (p.Val163Leu) rs55697431 0.00019
NM_004304.5(ALK):c.2478C>T (p.Tyr826=) rs142126984 0.00016
NM_004304.5(ALK):c.*45G>A rs186421480 0.00013
NM_004304.5(ALK):c.1111G>A (p.Ala371Thr) rs149968229 0.00011
NM_004304.5(ALK):c.2011C>T (p.Pro671Ser) rs145780832 0.00006
NM_004304.5(ALK):c.2127C>A (p.Asn709Lys) rs376175333 0.00003
NM_004304.5(ALK):c.4480G>A (p.Gly1494Arg) rs199940609 0.00002
NM_004304.5(ALK):c.-539G>A rs200662898
NM_004304.5(ALK):c.1720G>C (p.Gly574Arg) rs762358335
NM_004304.5(ALK):c.2775A>G (p.Gly925=) rs777406442
NM_004304.5(ALK):c.3600G>C (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.702T>A (p.Pro234=) rs2246745

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