ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.1851+2T>C

dbSNP: rs757785566
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MutSpliceDB: a database of splice sites variants effects on splicing, NIH RCV001844436 SCV002103330 not provided not provided no assertion provided research

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