List of variants reported as uncertain significance for colorectal cancer, susceptibility to, 12 by Baylor Genetics

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 87

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HGVS	dbSNP	gnomAD frequency
NM_006231.4(POLE):c.1184G>A (p.Gly395Glu)	rs546499094	0.00022
NM_006231.4(POLE):c.154C>T (p.Arg52Trp)	rs115452881	0.00016
NM_006231.4(POLE):c.3245G>A (p.Arg1082His)	rs201744227	0.00016
NM_006231.4(POLE):c.1064A>G (p.Lys355Arg)	rs141396559	0.00012
NM_006231.4(POLE):c.1282G>A (p.Ala428Thr)	rs150032060	0.00008
NM_006231.4(POLE):c.1868A>G (p.Tyr623Cys)	rs150564856	0.00008
NM_006231.4(POLE):c.926A>G (p.Asn309Ser)	rs767060387	0.00008
NM_006231.4(POLE):c.2645A>G (p.Asn882Ser)	rs539312991	0.00005
NM_006231.4(POLE):c.686A>C (p.His229Pro)	rs1482513360	0.00005
NM_006231.4(POLE):c.844C>T (p.Pro282Ser)	rs138207610	0.00005
NM_006231.4(POLE):c.1264C>T (p.His422Tyr)	rs745356467	0.00004
NM_006231.4(POLE):c.1336C>T (p.Arg446Trp)	rs200403177	0.00004
NM_006231.4(POLE):c.1411A>G (p.Met471Val)	rs749021187	0.00004
NM_006231.4(POLE):c.155G>A (p.Arg52Gln)	rs372459649	0.00004
NM_006231.4(POLE):c.863C>G (p.Ala288Gly)	rs771619667	0.00004
NM_006231.4(POLE):c.909G>C (p.Gln303His)	rs779801916	0.00004
NM_006231.4(POLE):c.1108C>A (p.Pro370Thr)	rs576578672	0.00003
NM_006231.4(POLE):c.1138G>T (p.Gly380Cys)	rs199746481	0.00003
NM_006231.4(POLE):c.1274A>G (p.Lys425Arg)	rs757186755	0.00003
NM_006231.4(POLE):c.5002G>A (p.Gly1668Ser)	rs371348453	0.00003
NM_006231.4(POLE):c.1055A>C (p.Gln352Pro)	rs766094330	0.00002
NM_006231.4(POLE):c.1181A>G (p.Gln394Arg)	rs1014444345	0.00002
NM_006231.4(POLE):c.1277C>T (p.Ala426Val)	rs374920539	0.00002
NM_006231.4(POLE):c.3698G>A (p.Arg1233Gln)	rs201738371	0.00002
NM_006231.4(POLE):c.850A>G (p.Lys284Glu)	rs568483856	0.00002
NM_006231.4(POLE):c.876G>T (p.Gln292His)	rs1324298673	0.00002
NM_006231.4(POLE):c.1041G>T (p.Trp347Cys)	rs1048183984	0.00001
NM_006231.4(POLE):c.1070C>T (p.Thr357Ile)	rs2043035482	0.00001
NM_006231.4(POLE):c.1078G>A (p.Val360Ile)	rs1315083272	0.00001
NM_006231.4(POLE):c.1124G>A (p.Arg375Gln)	rs778572159	0.00001
NM_006231.4(POLE):c.1193A>G (p.Lys398Arg)	rs1402549512	0.00001
NM_006231.4(POLE):c.1280C>T (p.Ala427Val)	rs878854841	0.00001
NM_006231.4(POLE):c.1309G>A (p.Val437Met)	rs115047349	0.00001
NM_006231.4(POLE):c.1346C>T (p.Thr449Met)	rs780299012	0.00001
NM_006231.4(POLE):c.1370C>T (p.Thr457Met)	rs878854842	0.00001
NM_006231.4(POLE):c.1378G>A (p.Val460Met)	rs753586583	0.00001
NM_006231.4(POLE):c.1384G>A (p.Asp462Asn)	rs765946486	0.00001
NM_006231.4(POLE):c.1396A>G (p.Thr466Ala)	rs761765763	0.00001
NM_006231.4(POLE):c.1420G>A (p.Val474Ile)	rs980578884	0.00001
NM_006231.4(POLE):c.1447A>G (p.Thr483Ala)	rs777736640	0.00001
NM_006231.4(POLE):c.6065G>A (p.Ser2022Asn)	rs905858506	0.00001
NM_006231.4(POLE):c.805C>G (p.Pro269Ala)	rs757438555	0.00001
NM_006231.4(POLE):c.811G>A (p.Val271Ile)	rs2043060448	0.00001
NM_006231.4(POLE):c.882G>A (p.Met294Ile)	rs774328855	0.00001
NM_006231.4(POLE):c.895A>G (p.Met299Val)	rs370727992	0.00001
NM_006231.4(POLE):c.901G>A (p.Asp301Asn)	rs1060500882	0.00001
NM_006231.4(POLE):c.902A>G (p.Asp301Gly)	rs1060500828	0.00001
NM_006231.4(POLE):c.974A>G (p.Lys325Arg)	rs1555229291	0.00001
NM_006231.4(POLE):c.1004T>C (p.Phe335Ser)
NM_006231.4(POLE):c.1008T>A (p.Asn336Lys)
NM_006231.4(POLE):c.1016A>T (p.Asp339Val)	rs1060500865
NM_006231.4(POLE):c.1021G>C (p.Ala341Pro)	rs137860861
NM_006231.4(POLE):c.1025A>G (p.His342Arg)	rs2136012061
NM_006231.4(POLE):c.1025A>T (p.His342Leu)	rs2136012061
NM_006231.4(POLE):c.1069A>G (p.Thr357Ala)	rs1593077507
NM_006231.4(POLE):c.1123C>T (p.Arg375Trp)	rs556789278
NM_006231.4(POLE):c.1129G>A (p.Ala377Thr)	rs754508108
NM_006231.4(POLE):c.1135C>T (p.His379Tyr)
NM_006231.4(POLE):c.1138G>A (p.Gly380Ser)	rs199746481
NM_006231.4(POLE):c.1142T>A (p.Leu381Gln)
NM_006231.4(POLE):c.1147A>G (p.Met383Val)	rs879254238
NM_006231.4(POLE):c.1156G>A (p.Glu386Lys)	rs893340262
NM_006231.4(POLE):c.1175A>G (p.Asp392Gly)	rs878854840
NM_006231.4(POLE):c.1182G>C (p.Gln394His)	rs2136008752
NM_006231.4(POLE):c.1232T>C (p.Val411Ala)	rs1031999052
NM_006231.4(POLE):c.1268A>G (p.Asn423Ser)
NM_006231.4(POLE):c.1294C>G (p.Leu432Val)	rs750475909
NM_006231.4(POLE):c.1324G>C (p.Glu442Gln)
NM_006231.4(POLE):c.1339A>C (p.Met447Leu)	rs376095661
NM_006231.4(POLE):c.1354C>A (p.Pro452Thr)	rs1555228573
NM_006231.4(POLE):c.1393G>T (p.Ala465Ser)	rs771526654
NM_006231.4(POLE):c.1439C>T (p.Ala480Val)	rs951851739
NM_006231.4(POLE):c.1453A>G (p.Ile485Val)	rs1593072187
NM_006231.4(POLE):c.1455T>G (p.Ile485Met)	rs878854843
NM_006231.4(POLE):c.2090C>A (p.Pro697His)	rs36120395
NM_006231.4(POLE):c.4558A>G (p.Ser1520Gly)	rs1021500357
NM_006231.4(POLE):c.825C>G (p.Asp275Glu)	rs1483809345
NM_006231.4(POLE):c.826A>G (p.Ile276Val)	rs1280169933
NM_006231.4(POLE):c.840A>C (p.Lys280Asn)	rs908089476
NM_006231.4(POLE):c.878T>C (p.Ile293Thr)	rs2136015678
NM_006231.4(POLE):c.883A>G (p.Met295Val)
NM_006231.4(POLE):c.916C>T (p.Leu306Phe)	rs1343048638
NM_006231.4(POLE):c.923C>T (p.Thr308Ile)
NM_006231.4(POLE):c.936T>G (p.Ile312Met)	rs1555229316
NM_006231.4(POLE):c.950T>C (p.Ile317Thr)	rs1060500783
NM_006231.4(POLE):c.968C>A (p.Thr323Asn)	rs1060500873
NM_006231.4(POLE):c.983A>T (p.Tyr328Phe)	rs1339375099

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