ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.2229C>T (p.Gly743=)

gnomAD frequency: 0.00015  dbSNP: rs111253753
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000470137 SCV000541820 likely benign Neuroblastoma, susceptibility to, 3 2024-01-28 criteria provided, single submitter clinical testing
Ambry Genetics RCV002429471 SCV002728884 likely benign Hereditary cancer-predisposing syndrome 2022-02-22 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: 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.
CeGaT Center for Human Genetics Tuebingen RCV003424009 SCV004144039 likely benign not provided 2023-07-01 criteria provided, single submitter clinical testing ALK: BP4, BP7

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