ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.1935_1936del (p.Gly646fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004795501 SCV005415976 pathogenic Acute myeloid leukemia; Tatton-Brown-Rahman overgrowth syndrome; Heyn-Sproul-Jackson syndrome criteria provided, single submitter clinical testing PVS1+PM2_Supporting+PS2_Supporting+PP4

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