ClinVar Miner

List of variants in gene ALK reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.4472A>G (p.Lys1491Arg) rs1881420 0.26767
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.1427T>C (p.Val476Ala) rs35093491 0.02566
NM_004304.5(ALK):c.4203T>C (p.Tyr1401=) rs55772745 0.01865
NM_004304.5(ALK):c.2039C>T (p.Thr680Ile) rs35228363 0.01598
NM_004304.5(ALK):c.-5G>A rs56270786 0.01336
NM_004304.5(ALK):c.645T>C (p.Leu215=) rs115392387 0.00889
NM_004304.5(ALK):c.1464C>T (p.Gly488=) rs56165377 0.00615
NM_004304.5(ALK):c.1719C>T (p.Thr573=) rs74830770 0.00577
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.776G>A (p.Arg259His) rs138686378 0.00096
NM_004304.5(ALK):c.4796C>A (p.Pro1599His) rs1881423 0.00091
NM_004304.5(ALK):c.2430C>T (p.Ser810=) rs150292405 0.00086
NM_004304.5(ALK):c.932G>A (p.Arg311His) rs150966028 0.00063
NM_004304.5(ALK):c.1277G>C (p.Ser426Thr) rs111796753 0.00054
NM_004304.5(ALK):c.3080C>T (p.Pro1027Leu) rs140733978 0.00054
NM_004304.5(ALK):c.2343C>T (p.Asp781=) rs61754933 0.00048
NM_004304.5(ALK):c.4255G>A (p.Glu1419Lys) rs56181542 0.00046
NM_004304.5(ALK):c.106C>T (p.Pro36Ser) rs201490095 0.00045
NM_004304.5(ALK):c.2451C>T (p.Gly817=) rs183314518 0.00039
NM_004304.5(ALK):c.1755C>T (p.Ala585=) rs373605278 0.00032
NM_004304.5(ALK):c.3102G>A (p.Ser1034=) rs138771319 0.00029
NM_004304.5(ALK):c.3291C>T (p.Cys1097=) rs370170353 0.00022
NM_004304.5(ALK):c.4185C>T (p.Thr1395=) rs571470900 0.00022
NM_004304.5(ALK):c.1584T>C (p.Ala528=) rs368877224 0.00021
NM_004304.5(ALK):c.3633C>A (p.Thr1211=) rs144437923 0.00021
NM_004304.5(ALK):c.3336G>A (p.Pro1112=) rs146074150 0.00019
NM_004304.5(ALK):c.4200A>C (p.Glu1400Asp) rs143647372 0.00018
NM_004304.5(ALK):c.174C>T (p.Phe58=) rs762994068 0.00016
NM_004304.5(ALK):c.2149G>A (p.Glu717Lys) rs147858673 0.00016
NM_004304.5(ALK):c.315G>A (p.Ala105=) rs897667874 0.00016
NM_004304.5(ALK):c.4275G>A (p.Leu1425=) rs749418931 0.00015
NM_004304.5(ALK):c.679T>C (p.Leu227=) rs201659891 0.00014
NM_004304.5(ALK):c.1528C>T (p.Arg510Trp) rs201449759 0.00013
NM_004304.5(ALK):c.1111G>A (p.Ala371Thr) rs149968229 0.00011
NM_004304.5(ALK):c.2928C>T (p.His976=) rs75895956 0.00011
NM_004304.5(ALK):c.2416C>T (p.Arg806Cys) rs80227749 0.00010
NM_004304.5(ALK):c.2632+8G>A rs199653862 0.00009
NM_004304.5(ALK):c.2504C>T (p.Pro835Leu) rs376091121 0.00008
NM_004304.5(ALK):c.3481G>A (p.Glu1161Lys) rs145194836 0.00008
NM_004304.5(ALK):c.1050G>A (p.Ser350=) rs749145522 0.00006
NM_004304.5(ALK):c.2633-3C>T rs200341945 0.00006
NM_004304.5(ALK):c.1107C>T (p.Asn369=) rs114429299 0.00005
NM_004304.5(ALK):c.3030C>T (p.His1010=) rs367642503 0.00005
NM_004304.5(ALK):c.1794G>A (p.Leu598=) rs942266375 0.00004
NM_004304.5(ALK):c.336C>G (p.Ala112=) rs776604754 0.00004
NM_004304.5(ALK):c.4811A>G (p.Tyr1604Cys) rs372440265 0.00004
NM_004304.5(ALK):c.2497G>T (p.Gly833Ter) rs74360487 0.00003
NM_004304.5(ALK):c.3210G>A (p.Gln1070=) rs138178848 0.00003
NM_004304.5(ALK):c.386G>T (p.Gly129Val) rs760041708 0.00003
NM_004304.5(ALK):c.4194G>A (p.Pro1398=) rs201653228 0.00003
NM_004304.5(ALK):c.4425C>T (p.His1475=) rs139039449 0.00003
NM_004304.5(ALK):c.4659C>A (p.Ala1553=) rs778797863 0.00003
NM_004304.5(ALK):c.919C>T (p.Pro307Ser) rs199790669 0.00003
NM_004304.5(ALK):c.1376A>G (p.Gln459Arg) rs773380015 0.00002
NM_004304.5(ALK):c.2487+4_2487+5insA rs755502856 0.00002
NM_004304.5(ALK):c.2895G>A (p.Leu965=) rs528928041 0.00002
NM_004304.5(ALK):c.4723C>T (p.Arg1575Cys) rs148351049 0.00002
NM_004304.5(ALK):c.107C>T (p.Pro36Leu) rs773691688 0.00001
NM_004304.5(ALK):c.1096C>T (p.Leu366=) rs1450281991 0.00001
NM_004304.5(ALK):c.171C>T (p.Asp57=) rs138165457 0.00001
NM_004304.5(ALK):c.1720G>A (p.Gly574Arg) rs762358335 0.00001
NM_004304.5(ALK):c.2110G>A (p.Ala704Thr) rs34829159 0.00001
NM_004304.5(ALK):c.2633-6C>T rs577768628 0.00001
NM_004304.5(ALK):c.2822A>G (p.Asn941Ser) rs368654781 0.00001
NM_004304.5(ALK):c.3228T>C (p.Pro1076=) rs199685862 0.00001
NM_004304.5(ALK):c.3812T>A (p.Phe1271Tyr) rs1348950153 0.00001
NM_004304.5(ALK):c.414C>G (p.Ala138=) rs1483565631 0.00001
NM_004304.5(ALK):c.4683G>A (p.Ser1561=) rs150487874 0.00001
NM_004304.5(ALK):c.-3G>C rs1031317995
NM_004304.5(ALK):c.1626G>A (p.Pro542=) rs143916398
NM_004304.5(ALK):c.1794G>T (p.Leu598Phe) rs942266375
NM_004304.5(ALK):c.2205-9C>G rs1046349000
NM_004304.5(ALK):c.2257C>T (p.Arg753Trp) rs745499366
NM_004304.5(ALK):c.2859A>G (p.Glu953=)
NM_004304.5(ALK):c.3521T>G (p.Phe1174Cys) rs1057519697
NM_004304.5(ALK):c.3600G>A (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.4682C>T (p.Ser1561Leu) rs1209157216
NM_004304.5(ALK):c.62C>T (p.Ser21Phe)
NM_004304.5(ALK):c.702T>A (p.Pro234=) rs2246745
NM_004304.5(ALK):c.702T>G (p.Pro234=) rs2246745
NM_004304.5(ALK):c.781C>T (p.Arg261Ter) rs972790555
NM_004304.5(ALK):c.782G>A (p.Arg261Gln) rs375097381
NM_004304.5(ALK):c.861C>T (p.Ser287=) rs1321970113

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.