ClinVar Miner

List of variants in gene ALK studied for Neuroblastoma Susceptibility

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP
NM_004304.4(ALK):c.*111C>T rs74669215
NM_004304.4(ALK):c.*185C>T rs547955328
NM_004304.4(ALK):c.*189T>C rs886055926
NM_004304.4(ALK):c.*298C>T rs1728828
NM_004304.4(ALK):c.*415G>A rs886055925
NM_004304.4(ALK):c.*45G>A rs186421480
NM_004304.4(ALK):c.*53G>C rs80088378
NM_004304.4(ALK):c.*61_*64dupCAAT rs397706189
NM_004304.4(ALK):c.*62_*65dupAATG rs886055927
NM_004304.4(ALK):c.*63A>G rs182561050
NM_004304.4(ALK):c.-156G>T rs141444957
NM_004304.4(ALK):c.-161T>C rs886055934
NM_004304.4(ALK):c.-273G>C rs72857538
NM_004304.4(ALK):c.-276G>A rs886055935
NM_004304.4(ALK):c.-292G>A rs578166431
NM_004304.4(ALK):c.-312G>T rs886055936
NM_004304.4(ALK):c.-313C>G rs72857540
NM_004304.4(ALK):c.-403G>A rs572286447
NM_004304.4(ALK):c.-415T>C rs755231246
NM_004304.4(ALK):c.-566G>T rs886055937
NM_004304.4(ALK):c.-5G>A rs56270786
NM_004304.4(ALK):c.-624C>G rs886055938
NM_004304.4(ALK):c.-751C>T rs547587734
NM_004304.4(ALK):c.-826C>A rs886055939
NM_004304.4(ALK):c.106C>T (p.Pro36Ser) rs201490095
NM_004304.4(ALK):c.1111G>A (p.Ala371Thr) rs149968229
NM_004304.4(ALK):c.1249G>A (p.Val417Met) rs886055931
NM_004304.4(ALK):c.1427T>C (p.Val476Ala) rs35093491
NM_004304.4(ALK):c.1464C>T (p.Gly488=) rs56165377
NM_004304.4(ALK):c.1500A>G (p.Gln500=) rs2293564
NM_004304.4(ALK):c.1550A>G (p.His517Arg) rs367674546
NM_004304.4(ALK):c.1626G>C (p.Pro542=) rs143916398
NM_004304.4(ALK):c.2011C>T (p.Pro671Ser) rs145780832
NM_004304.4(ALK):c.2039C>T (p.Thr680Ile) rs35228363
NM_004304.4(ALK):c.2109C>T (p.Asn703=) rs560163657
NM_004304.4(ALK):c.2127C>A (p.Asn709Lys) rs376175333
NM_004304.4(ALK):c.2133C>T (p.Ser711=) rs77102810
NM_004304.4(ALK):c.2148C>T (p.Ser716=) rs55733526
NM_004304.4(ALK):c.2175C>T (p.Ile725=) rs57881134
NM_004304.4(ALK):c.2210C>T (p.Ser737Leu) rs368581969
NM_004304.4(ALK):c.2430C>T (p.Ser810=) rs150292405
NM_004304.4(ALK):c.2488A>T (p.Met830Leu) rs780536554
NM_004304.4(ALK):c.2526C>T (p.Ala842=) rs145271283
NM_004304.4(ALK):c.2535T>C (p.Gly845=) rs2256740
NM_004304.4(ALK):c.2603T>A (p.Leu868Gln) rs55941323
NM_004304.4(ALK):c.2613C>T (p.Asn871=) rs150557024
NM_004304.4(ALK):c.2676C>T (p.Ala892=) rs138668699
NM_004304.4(ALK):c.27C>G (p.Leu9=) rs4358080
NM_004304.4(ALK):c.2901C>A (p.Thr967=) rs886055930
NM_004304.4(ALK):c.3035C>T (p.Thr1012Met) rs35073634
NM_004304.4(ALK):c.3036G>A (p.Thr1012=) rs2293563
NM_004304.4(ALK):c.3057C>A (p.Val1019=) rs138406372
NM_004304.4(ALK):c.3085C>G (p.Pro1029Ala) rs543328121
NM_004304.4(ALK):c.310C>A (p.Pro104Thr) rs576431612
NM_004304.4(ALK):c.3173-11C>T rs79339096
NM_004304.4(ALK):c.32C>T (p.Pro11Leu) rs767822322
NM_004304.4(ALK):c.3336G>A (p.Pro1112=) rs146074150
NM_004304.4(ALK):c.3359+6C>T rs4622670
NM_004304.4(ALK):c.3375C>A (p.Gly1125=) rs3795850
NM_004304.4(ALK):c.3408C>T (p.Ser1136=) rs56146053
NM_004304.4(ALK):c.3594C>T (p.Leu1198=) rs56071005
NM_004304.4(ALK):c.3600G>C (p.Ala1200=) rs56247462
NM_004304.4(ALK):c.3633C>A (p.Thr1211=) rs144437923
NM_004304.4(ALK):c.3839C>T (p.Ala1280Val) rs74716434
NM_004304.4(ALK):c.384G>A (p.Lys128=) rs753267950
NM_004304.4(ALK):c.386G>T (p.Gly129Val) rs760041708
NM_004304.4(ALK):c.3939-8A>G rs3738869
NM_004304.4(ALK):c.4165-6C>T rs17007646
NM_004304.4(ALK):c.4186G>A (p.Ala1396Thr) rs201768549
NM_004304.4(ALK):c.4203T>C (p.Tyr1401=) rs55772745
NM_004304.4(ALK):c.4255G>A (p.Glu1419Lys) rs56181542
NM_004304.4(ALK):c.4303_4305delGAG (p.Glu1435del) rs138827116
NM_004304.4(ALK):c.4338C>T (p.Thr1446=) rs56132472
NM_004304.4(ALK):c.4344C>T (p.Ser1448=) rs886055929
NM_004304.4(ALK):c.4375G>T (p.Ala1459Ser) rs372612147
NM_004304.4(ALK):c.4381A>G (p.Ile1461Val) rs1670283
NM_004304.4(ALK):c.4433T>C (p.Met1478Thr) rs141010693
NM_004304.4(ALK):c.4472A>G (p.Lys1491Arg) rs1881420
NM_004304.4(ALK):c.4573A>G (p.Lys1525Glu) rs139437088
NM_004304.4(ALK):c.4587C>G (p.Asp1529Glu) rs1881421
NM_004304.4(ALK):c.4596C>T (p.Asn1532=) rs1881422
NM_004304.4(ALK):c.4648C>G (p.Leu1550Val) rs886055928
NM_004304.4(ALK):c.4836G>A (p.Lys1612=) rs78174819
NM_004304.4(ALK):c.507T>C (p.Asn169=) rs780271684
NM_004304.4(ALK):c.510C>T (p.Leu170=) rs886055933
NM_004304.4(ALK):c.597C>T (p.Gly199=) rs200868013
NM_004304.4(ALK):c.645T>C (p.Leu215=) rs115392387
NM_004304.4(ALK):c.655A>G (p.Ile219Val) rs886055932
NM_004304.4(ALK):c.702T>A (p.Pro234=) rs2246745
NM_004304.4(ALK):c.72G>A (p.Gly24=) rs756782371
NM_004304.4(ALK):c.930G>T (p.Glu310Asp) rs367712624

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.