ClinVar Miner

Submissions for variant NM_001126112.2(TP53):c.919+1G>T (rs1131691039)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Sciences Centre,British Columbia Cancer Agency RCV000586000 SCV000693732 likely pathogenic Malignant Colorectal Neoplasm 2016-07-11 no assertion criteria provided research
MutSpliceDB: a database of splice sites variants effects on splicing,NIH RCV000786817 SCV000925710 not provided not provided no assertion provided in vitro

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