List of variants reported as pathogenic for Familial colorectal cancer by OMIM

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.566C>T (p.Ala189Val)	rs121912665	0.00001
NM_000546.6(TP53):c.974G>T (p.Gly325Val)	rs121912659	0.00001
NC_012920.1(MT-CO1):m.6264G>A	rs267606882
NC_012920.1(MT-CO1):m.6277G>A	rs281865417
NC_012920.1(MT-CO1):m.7275T>C	rs267606884
NC_012920.1(MT-CO2):m.8009G>A	rs199474826
NC_012920.1(MT-CYB):m.14985G>A	rs207459995
NC_012920.1(MT-CYB):m.15572T>C	rs207459996
NC_012920.1(MT-ND4L):m.10563T>C	rs267606892
NM_001395463.1(PLA2G2A):c.144_145del (p.Cys48fs)	rs587776800

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