ClinVar Miner

List of variants in gene ALK reported as uncertain significance for Neuroblastoma Susceptibility

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_004304.5(ALK):c.*185C>T rs547955328
NM_004304.5(ALK):c.*189T>C rs886055926
NM_004304.5(ALK):c.*415G>A rs886055925
NM_004304.5(ALK):c.*62_*65dup rs886055927
NM_004304.5(ALK):c.-161T>C rs886055934
NM_004304.5(ALK):c.-276G>A rs886055935
NM_004304.5(ALK):c.-292G>A rs578166431
NM_004304.5(ALK):c.-312G>T rs886055936
NM_004304.5(ALK):c.-403G>A rs572286447
NM_004304.5(ALK):c.-415T>C rs755231246
NM_004304.5(ALK):c.-566G>T rs886055937
NM_004304.5(ALK):c.-624C>G rs886055938
NM_004304.5(ALK):c.-751C>T rs547587734
NM_004304.5(ALK):c.-826C>A rs886055939
NM_004304.5(ALK):c.1249G>A (p.Val417Met) rs886055931
NM_004304.5(ALK):c.1550A>G (p.His517Arg) rs367674546
NM_004304.5(ALK):c.1626G>C (p.Pro542=) rs143916398
NM_004304.5(ALK):c.2210C>T (p.Ser737Leu) rs368581969
NM_004304.5(ALK):c.2488A>T (p.Met830Leu) rs780536554
NM_004304.5(ALK):c.2603T>A (p.Leu868Gln) rs55941323
NM_004304.5(ALK):c.2901C>A (p.Thr967=) rs886055930
NM_004304.5(ALK):c.3173-11C>T rs79339096
NM_004304.5(ALK):c.32C>T (p.Pro11Leu) rs767822322
NM_004304.5(ALK):c.3633C>A (p.Thr1211=) rs144437923
NM_004304.5(ALK):c.384G>A (p.Lys128=) rs753267950
NM_004304.5(ALK):c.386G>T (p.Gly129Val) rs760041708
NM_004304.5(ALK):c.4186G>A (p.Ala1396Thr) rs201768549
NM_004304.5(ALK):c.4344C>T (p.Ser1448=) rs886055929
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.597C>T (p.Gly199=) rs200868013
NM_004304.5(ALK):c.655A>G (p.Ile219Val) rs886055932
NM_004304.5(ALK):c.72G>A (p.Gly24=) rs756782371
NM_004304.5(ALK):c.930G>T (p.Glu310Asp) rs367712624

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