ClinVar Miner

List of variants in gene ALK studied for carcinoma

Included ClinVar conditions (235):
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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_004304.5(ALK):c.4381A>G (p.Ile1461Val) rs1670283 0.99030
NM_004304.5(ALK):c.4587C>G (p.Asp1529Glu) rs1881421 0.47503
NM_004304.5(ALK):c.3375C>A (p.Gly1125=) rs3795850 0.27292
NM_004304.5(ALK):c.3359+24G>C rs2276550 0.26990
NM_004304.5(ALK):c.4472A>G (p.Lys1491Arg) rs1881420 0.26767
NM_004304.5(ALK):c.4165-6C>T rs17007646 0.20768
NM_004304.5(ALK):c.4338C>T (p.Thr1446=) rs56132472 0.10831
NM_004304.5(ALK):c.2205-116G>A
NM_004304.5(ALK):c.3098T>A (p.Leu1033His) rs572614173
NM_004304.5(ALK):c.3451-35TCC[3] rs775243091
NM_004304.5(ALK):c.3455T>G (p.Leu1152Arg) rs1057519785
NM_004304.5(ALK):c.3467G>A (p.Cys1156Tyr) rs1057519859
NM_004304.5(ALK):c.3522C>A (p.Phe1174Leu) rs863225281
NM_004304.5(ALK):c.3522C>G (p.Phe1174Leu) rs863225281
NM_004304.5(ALK):c.3586C>A (p.Leu1196Met) rs1057519784
NM_004304.5(ALK):c.3604G>A (p.Gly1202Arg) rs1057519783
NM_004304.5(ALK):c.3617C>A (p.Ser1206Tyr) rs1057519782
NM_004304.5(ALK):c.3744-53del rs1669420011
NM_004304.5(ALK):c.3806G>C (p.Gly1269Ala) rs1057519781
NM_004304.5(ALK):c.4165-19del rs1668958808
Single allele

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