ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004304.5(ALK):c.-415T>C rs755231246 0.00057
NM_004304.5(ALK):c.469C>T (p.Pro157Ser) rs74774946 0.00055
NM_004304.5(ALK):c.-751C>T rs547587734 0.00033
NM_004304.5(ALK):c.3257C>T (p.Ser1086Leu) rs138589984 0.00018
NM_004304.5(ALK):c.4200A>C (p.Glu1400Asp) rs143647372 0.00018
NM_004304.5(ALK):c.*185C>T rs547955328 0.00016
NM_004304.5(ALK):c.-896C>T rs1020153617 0.00014
NM_004304.5(ALK):c.3173-11C>T rs79339096 0.00013
NM_004304.5(ALK):c.3599C>T (p.Ala1200Val) rs200585833 0.00011
NM_004304.5(ALK):c.-161T>C rs886055934 0.00009
NM_004304.5(ALK):c.-490C>T rs957194330 0.00009
NM_004304.5(ALK):c.-566G>T rs886055937 0.00008
NM_004304.5(ALK):c.3362G>A (p.Gly1121Asp) rs55760835 0.00008
NM_004304.5(ALK):c.3115G>A (p.Val1039Met) rs200080181 0.00007
NM_004304.5(ALK):c.2479G>A (p.Val827Ile) rs756963896 0.00005
NM_004304.5(ALK):c.1044C>T (p.Ala348=) rs200293454 0.00004
NM_004304.5(ALK):c.1670G>A (p.Arg557His) rs200468507 0.00004
NM_004304.5(ALK):c.32C>T (p.Pro11Leu) rs767822322 0.00004
NM_004304.5(ALK):c.930G>T (p.Glu310Asp) rs367712624 0.00004
NM_004304.5(ALK):c.-624C>G rs886055938 0.00003
NM_004304.5(ALK):c.-830C>T rs1227238002 0.00003
NM_004304.5(ALK):c.2452G>A (p.Gly818Arg) rs777803249 0.00003
NM_004304.5(ALK):c.4425C>T (p.His1475=) rs139039449 0.00003
NM_004304.5(ALK):c.615C>G (p.Ser205=) rs567498111 0.00003
NM_004304.5(ALK):c.*189T>C rs886055926 0.00002
NM_004304.5(ALK):c.1049C>T (p.Ser350Leu) rs759426382 0.00002
NM_004304.5(ALK):c.3574C>T (p.Arg1192Trp) rs534852056 0.00002
NM_004304.5(ALK):c.3939-9C>T rs749848775 0.00002
NM_004304.5(ALK):c.4210C>G (p.Leu1404Val) rs757615099 0.00002
NM_004304.5(ALK):c.-128A>G rs1246468331 0.00001
NM_004304.5(ALK):c.-276G>A rs886055935 0.00001
NM_004304.5(ALK):c.-403G>A rs572286447 0.00001
NM_004304.5(ALK):c.-699A>G rs943046273 0.00001
NM_004304.5(ALK):c.1908C>G (p.Leu636=) rs1268649558 0.00001
NM_004304.5(ALK):c.2304T>C (p.Asp768=) rs758649392 0.00001
NM_004304.5(ALK):c.2488A>T (p.Met830Leu) rs780536554 0.00001
NM_004304.5(ALK):c.2579G>T (p.Arg860Ile) rs1194282326 0.00001
NM_004304.5(ALK):c.2603T>A (p.Leu868Gln) rs55941323 0.00001
NM_004304.5(ALK):c.2740G>A (p.Gly914Arg) rs1220052371 0.00001
NM_004304.5(ALK):c.3524A>G (p.Asn1175Ser) rs774872969 0.00001
NM_004304.5(ALK):c.357G>T (p.Glu119Asp) rs758250431 0.00001
NM_004304.5(ALK):c.3958T>C (p.Trp1320Arg) rs779796155 0.00001
NM_004304.5(ALK):c.4344C>T (p.Ser1448=) rs886055929 0.00001
NM_004304.5(ALK):c.4608G>A (p.Glu1536=) rs147241767 0.00001
NM_004304.5(ALK):c.4809T>C (p.His1603=) rs758502850 0.00001
NM_004304.5(ALK):c.655A>G (p.Ile219Val) rs886055932 0.00001
NM_004304.5(ALK):c.843T>A (p.His281Gln) rs759250272 0.00001
NM_004304.5(ALK):c.*246G>A rs1668908633
NM_004304.5(ALK):c.*403T>C rs1668903533
NM_004304.5(ALK):c.*407A>C rs1668903341
NM_004304.5(ALK):c.*415G>A rs886055925
NM_004304.5(ALK):c.*62_*65dup rs886055927
NM_004304.5(ALK):c.-292G>A rs578166431
NM_004304.5(ALK):c.-312G>T rs886055936
NM_004304.5(ALK):c.-376G>A rs1254508871
NM_004304.5(ALK):c.-611G>A rs1667997371
NM_004304.5(ALK):c.-61C>T rs1052528841
NM_004304.5(ALK):c.-826C>A rs886055939
NM_004304.5(ALK):c.-922C>A rs372410498
NM_004304.5(ALK):c.1249G>A (p.Val417Met) rs886055931
NM_004304.5(ALK):c.1306G>A (p.Ala436Thr) rs745772939
NM_004304.5(ALK):c.139T>G (p.Ser47Ala) rs1402352282
NM_004304.5(ALK):c.1507G>A (p.Val503Ile) rs1229156257
NM_004304.5(ALK):c.1890C>T (p.Ile630=) rs1278070199
NM_004304.5(ALK):c.2065G>C (p.Gly689Arg) rs1664809619
NM_004304.5(ALK):c.2073C>T (p.Ser691=) rs370435082
NM_004304.5(ALK):c.224C>A (p.Pro75Gln) rs1667963680
NM_004304.5(ALK):c.2901C>A (p.Thr967=) rs886055930
NM_004304.5(ALK):c.310C>A (p.Pro104Thr) rs576431612
NM_004304.5(ALK):c.3260C>A (p.Thr1087Asn) rs113994090
NM_004304.5(ALK):c.3680T>C (p.Leu1227Pro) rs1669534712
NM_004304.5(ALK):c.4648C>G (p.Leu1550Val) rs886055928
NM_004304.5(ALK):c.507T>C (p.Asn169=) rs780271684
NM_004304.5(ALK):c.510C>T (p.Leu170=) rs886055933
NM_004304.5(ALK):c.615C>A (p.Ser205=) rs567498111
NM_004304.5(ALK):c.660C>T (p.Phe220=) rs1667944556
NM_004304.5(ALK):c.822G>A (p.Leu274=) rs1265006535

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.