ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3777T>C (p.Cys1259=)

dbSNP: rs1573102854
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001021112 SCV001182688 likely benign Hereditary cancer-predisposing syndrome 2018-02-06 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV002069012 SCV002476203 likely benign Neuroblastoma, susceptibility to, 3 2023-08-24 criteria provided, single submitter clinical testing

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