ClinVar Miner

Submissions for variant NM_003070.5(SMARCA2):c.3638G>C (p.Arg1213Pro)

dbSNP: rs1314729940
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Sciences Centre, British Columbia Cancer Agency RCV000585737 SCV000693668 uncertain significance Adenoid cystic carcinoma 2018-02-01 no assertion criteria provided research

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