ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.719G>A (p.Ser240Asn)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cancer Genetics Lab, University of Education RCV003229539 SCV003926523 pathogenic Acute myeloid leukemia no assertion criteria provided clinical testing

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