ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1799_1800delinsAT (p.Val600Asp)

dbSNP: rs121913377
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000423512 SCV000504246 pathogenic Melanoma 2015-07-14 no assertion criteria provided literature only

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