ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3538G>C (p.Val1180Leu)

dbSNP: rs2148166660
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molekularpathologisches Zentrum, Universitaetsklinikum Heidelberg RCV002283356 SCV002571104 likely pathogenic Lung cancer no assertion criteria provided clinical testing

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