ClinVar Miner

List of variants reported as likely pathogenic for colonic neoplasm by Database of Curated Mutations (DoCM)

Included ClinVar conditions (10):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001982.4(ERBB3):c.850G>A (p.Gly284Arg)	rs1057519803
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022
NM_004333.6(BRAF):c.1799_1800delinsAA (p.Val600Glu)	rs121913377

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