ClinVar Miner

Submissions for variant NM_152641.4(ARID2):c.2989C>T (p.Gln997Ter)

dbSNP: rs1555155110
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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 RCV000585750 SCV000693663 likely pathogenic Adenoid cystic carcinoma 2018-02-01 no assertion criteria provided research Truncating mutation in known tumour suppressor.

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