ClinVar Miner

Submissions for variant NM_005085.4(NUP214):c.5251A>G (p.Ser1751Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005043865 SCV005674879 uncertain significance Acute lymphoid leukemia; Acute myeloid leukemia; Encephalopathy, acute, infection-induced, susceptibility to, 9 2024-06-11 criteria provided, single submitter clinical testing

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