ClinVar Miner

Submissions for variant NM_000397.4(CYBB):c.937AAG[2] (p.Lys315del)

dbSNP: rs2146817067
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001564955 SCV001788204 pathogenic not provided 2021-06-21 criteria provided, single submitter clinical testing Published functional studies demonstrate a damaging effect on NADPH oxidase activity (Beaumel S et al., 2014); In-frame deletion of 1 amino acids in a non-repeat region; Not observed at significant frequency in large population cohorts (Lek et al., 2016); In silico analysis supports a deleterious effect on protein structure/function; This variant is associated with the following publications: (PMID: 7579466, 20729109, 26210446, 9585602, 15693794, 15777347, 25252997, 27535533)

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