ClinVar Miner

List of variants in gene ALK reported by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Gene type:
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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_004304.5(ALK):c.3837-9_3837-7dup rs373764155 0.00279
NM_004304.5(ALK):c.1100C>G (p.Pro367Arg) rs144030155 0.00023
NM_004304.5(ALK):c.1148A>T (p.Lys383Met) rs140928266 0.00020
NM_004304.5(ALK):c.470C>T (p.Pro157Leu) rs775385954 0.00013
NM_004304.5(ALK):c.4795C>T (p.Pro1599Ser) rs373037272 0.00013
NM_004304.5(ALK):c.1283-5T>C rs377214413 0.00012
NM_004304.5(ALK):c.1390G>A (p.Gly464Arg) rs55706535 0.00009
NM_004304.5(ALK):c.1550A>G (p.His517Arg) rs367674546 0.00008
NM_004304.5(ALK):c.3115G>A (p.Val1039Met) rs200080181 0.00007
NM_004304.5(ALK):c.3160G>A (p.Gly1054Ser) rs375889530 0.00007
NM_004304.5(ALK):c.1184G>A (p.Arg395His) rs769910087 0.00006
NM_004304.5(ALK):c.2633-3C>T rs200341945 0.00006
NM_004304.5(ALK):c.3031G>A (p.Gly1011Arg) rs587778021 0.00005
NM_004304.5(ALK):c.350C>G (p.Pro117Arg) rs201290745 0.00005
NM_004304.5(ALK):c.2194G>A (p.Asp732Asn) rs768366852 0.00003
NM_004304.5(ALK):c.298A>G (p.Arg100Gly) rs764559656 0.00003
NM_004304.5(ALK):c.1582G>A (p.Ala528Thr) rs758494304 0.00002
NM_004304.5(ALK):c.4210C>G (p.Leu1404Val) rs757615099 0.00002
NM_004304.5(ALK):c.1193A>G (p.Asn398Ser) rs754512910 0.00001
NM_004304.5(ALK):c.2302G>A (p.Asp768Asn) rs766666105 0.00001
NM_004304.5(ALK):c.3271G>A (p.Asp1091Asn) rs864309584 0.00001
NM_004304.5(ALK):c.699G>A (p.Met233Ile) rs778129557 0.00001
NM_004304.5(ALK):c.1517T>C (p.Leu506Pro) rs762569153
NM_004304.5(ALK):c.164C>A (p.Ala55Glu) rs1217013970
NM_004304.5(ALK):c.1875T>G (p.Phe625Leu) rs1553402765
NM_004304.5(ALK):c.3359+4A>G rs1573125072
NM_004304.5(ALK):c.4306C>T (p.Arg1436Cys) rs201129468
NM_004304.5(ALK):c.4442C>T (p.Ser1481Phe) rs1356575388
NM_004304.5(ALK):c.448A>C (p.Ile150Leu) rs1203267790

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