ClinVar Miner

List of variants reported as likely pathogenic for Colon cancer

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_001048174.2(MUTYH):c.464G>A (p.Gly155Asp)	rs587781864	0.00001
NM_000249.4(MLH1):c.374C>A (p.Ala125Glu)	rs1553641362

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