ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2054T>G (p.Val685Gly)

dbSNP: rs796052548
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000187641 SCV000241238 pathogenic not provided 2018-05-08 criteria provided, single submitter clinical testing The V685G variant in the GRIN2A gene has been reported previously in an individual with severe intractable epilepsy and global developmental delay (Swanger et al., 2016). The V685G variant is not observed in large population cohorts (Lek et al., 2016). The V685G variant is a conservative amino acid substitution in the agonist binding domain. Functional studies demonstrate that the V685G variant results in loss of normal protein function (Swanger et al., 2016). We interpret V685G as a pathogenic variant.

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