ClinVar Miner

Submissions for variant NM_032242.4(PLXNA1):c.2640G>A (p.Thr880=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003058623 SCV003447732 benign not provided 2022-06-10 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003963575 SCV004780893 likely benign PLXNA1-related disorder 2021-12-29 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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