List of variants reported as likely benign for colorectal cancer, susceptibility to, 12 by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_006231.4(POLE):c.1359+18C>T	rs5744775	0.00455
NM_006231.4(POLE):c.5811+16T>C	rs115381003	0.00423
NM_006231.4(POLE):c.-29C>G	rs571026345	0.00281
NM_006231.4(POLE):c.63-14C>T	rs373998767	0.00048
NM_006231.4(POLE):c.3379-12C>T	rs187618435	0.00023
NM_006231.4(POLE):c.6006G>A (p.Ala2002=)	rs146902214	0.00019
NM_006231.4(POLE):c.1226+13G>A	rs577646338	0.00011
NM_006231.4(POLE):c.2174-11G>A	rs111570840	0.00009
NM_006231.4(POLE):c.4011C>T (p.Ser1337=)	rs756716850	0.00005
NM_006231.4(POLE):c.4952+11T>A	rs779889181	0.00005
NM_006231.4(POLE):c.4150-6C>T	rs756837862	0.00004
NM_006231.4(POLE):c.555C>T (p.Asp185=)	rs763871536	0.00004
NM_006231.4(POLE):c.4269C>T (p.Ile1423=)	rs761413102	0.00003
NM_006231.4(POLE):c.5313G>A (p.Thr1771=)	rs201803493	0.00003
NM_006231.4(POLE):c.6321C>T (p.Tyr2107=)	rs201656807	0.00003
NM_006231.4(POLE):c.2343G>A (p.Ala781=)	rs199751241	0.00002
NM_006231.4(POLE):c.318T>C (p.Ile106=)	rs770759936	0.00002
NM_006231.4(POLE):c.4602C>T (p.His1534=)	rs749126952	0.00001
NM_006231.4(POLE):c.4744C>T (p.Pro1582Ser)	rs556887600	0.00001
NM_006231.4(POLE):c.5046C>T (p.His1682=)	rs769284070	0.00001
NM_006231.4(POLE):c.1781C>T (p.Thr594Ile)	rs574033788
NM_006231.4(POLE):c.2118C>T (p.Ala706=)	rs1555227247
NM_006231.4(POLE):c.4158G>A (p.Arg1386=)	rs1473134331
NM_006231.4(POLE):c.6658-19C>G	rs5745081
NM_006231.4(POLE):c.802-6C>T	rs754779082

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