ClinVar Miner

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

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_001982.3(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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