ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1387A>G (p.Ile463Val)

dbSNP: rs1562957000
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714710 SCV000845436 likely pathogenic Noonan syndrome 7 2018-08-07 criteria provided, single submitter clinical testing

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