ClinVar Miner

List of variants reported as uncertain significance for Colorectal cancer by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 244
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HGVS dbSNP gnomAD frequency
NM_182643.3(DLC1):c.1700C>T (p.Pro567Leu) rs139415835 0.00018
NM_182643.3(DLC1):c.857A>G (p.Asn286Ser) rs374190119 0.00005
NM_182643.3(DLC1):c.4274G>A (p.Arg1425Gln) rs377127652 0.00004
NM_182643.3(DLC1):c.4582A>T (p.Arg1528Trp) rs759626631 0.00001
NM_182643.3(DLC1):c.1007G>C (p.Arg336Thr)
NM_182643.3(DLC1):c.1009C>G (p.Leu337Val)
NM_182643.3(DLC1):c.1021A>C (p.Lys341Gln)
NM_182643.3(DLC1):c.1040G>C (p.Arg347Pro)
NM_182643.3(DLC1):c.1049C>A (p.Ala350Glu)
NM_182643.3(DLC1):c.1049C>T (p.Ala350Val)
NM_182643.3(DLC1):c.1077T>G (p.Ile359Met)
NM_182643.3(DLC1):c.1084C>T (p.Leu362=)
NM_182643.3(DLC1):c.1086G>T (p.Leu362=)
NM_182643.3(DLC1):c.1096G>C (p.Asp366His)
NM_182643.3(DLC1):c.1106T>C (p.Ile369Thr)
NM_182643.3(DLC1):c.112G>A (p.Asp38Asn)
NM_182643.3(DLC1):c.1135C>G (p.Pro379Ala)
NM_182643.3(DLC1):c.1160G>A (p.Arg387Gln)
NM_182643.3(DLC1):c.1167C>A (p.His389Gln)
NM_182643.3(DLC1):c.1173+6C>T
NM_182643.3(DLC1):c.1175A>T (p.Asp392Val)
NM_182643.3(DLC1):c.117C>A (p.Ser39Arg)
NM_182643.3(DLC1):c.1187G>T (p.Gly396Val)
NM_182643.3(DLC1):c.1189T>C (p.Ser397Pro)
NM_182643.3(DLC1):c.1219A>T (p.Asn407Tyr)
NM_182643.3(DLC1):c.1227_1237delinsTCAG (p.Arg410fs)
NM_182643.3(DLC1):c.1228C>T (p.Arg410Ter)
NM_182643.3(DLC1):c.1229G>A (p.Arg410Gln)
NM_182643.3(DLC1):c.122A>G (p.Gln41Arg)
NM_182643.3(DLC1):c.1237T>A (p.Leu413Met)
NM_182643.3(DLC1):c.1245T>A (p.Ser415=)
NM_182643.3(DLC1):c.1246G>C (p.Asp416His)
NM_182643.3(DLC1):c.1261G>A (p.Asp421Asn)
NM_182643.3(DLC1):c.1274C>T (p.Ser425Phe)
NM_182643.3(DLC1):c.1281A>G (p.Pro427=)
NM_182643.3(DLC1):c.1285G>C (p.Ala429Pro)
NM_182643.3(DLC1):c.1297A>G (p.Thr433Ala)
NM_182643.3(DLC1):c.1313C>T (p.Thr438Met)
NM_182643.3(DLC1):c.1314G>A (p.Thr438=)
NM_182643.3(DLC1):c.1321C>G (p.Gln441Glu)
NM_182643.3(DLC1):c.1337A>C (p.Lys446Thr)
NM_182643.3(DLC1):c.1360A>C (p.Lys454Gln)
NM_182643.3(DLC1):c.1370G>C (p.Cys457Ser)
NM_182643.3(DLC1):c.1382G>A (p.Arg461Gln)
NM_182643.3(DLC1):c.1419A>G (p.Glu473=)
NM_182643.3(DLC1):c.1421-5C>T
NM_182643.3(DLC1):c.1437C>A (p.Ile479=)
NM_182643.3(DLC1):c.1448T>C (p.Leu483Ser)
NM_182643.3(DLC1):c.1480G>C (p.Asp494His)
NM_182643.3(DLC1):c.1491G>C (p.Glu497Asp)
NM_182643.3(DLC1):c.1503G>A (p.Arg501=)
NM_182643.3(DLC1):c.1514C>T (p.Thr505Ile)
NM_182643.3(DLC1):c.1559G>A (p.Arg520Gln)
NM_182643.3(DLC1):c.1566+17_1566+18delinsGG
NM_182643.3(DLC1):c.1573G>A (p.Asp525Asn)
NM_182643.3(DLC1):c.1616C>T (p.Thr539Ile)
NM_182643.3(DLC1):c.161G>A (p.Arg54His)
NM_182643.3(DLC1):c.1683C>G (p.Asp561Glu)
NM_182643.3(DLC1):c.1684C>G (p.Leu562Val)
NM_182643.3(DLC1):c.1715C>G (p.Pro572Arg)
NM_182643.3(DLC1):c.1715C>T (p.Pro572Leu)
NM_182643.3(DLC1):c.1723G>C (p.Gly575Arg)
NM_182643.3(DLC1):c.1732C>A (p.Pro578Thr)
NM_182643.3(DLC1):c.173G>C (p.Cys58Ser)
NM_182643.3(DLC1):c.1753C>T (p.Leu585Phe)
NM_182643.3(DLC1):c.1758C>G (p.Ser586Arg)
NM_182643.3(DLC1):c.1774T>C (p.Ser592Pro)
NM_182643.3(DLC1):c.1793G>T (p.Ser598Ile)
NM_182643.3(DLC1):c.1795A>C (p.Ser599Arg)
NM_182643.3(DLC1):c.1818C>G (p.His606Gln)
NM_182643.3(DLC1):c.1826C>G (p.Pro609Arg)
NM_182643.3(DLC1):c.182T>C (p.Leu61Pro)
NM_182643.3(DLC1):c.1831G>C (p.Glu611Gln)
NM_182643.3(DLC1):c.1857C>T (p.Asn619=)
NM_182643.3(DLC1):c.1870G>T (p.Val624Phe)
NM_182643.3(DLC1):c.1877C>T (p.Ser626Phe)
NM_182643.3(DLC1):c.1912G>A (p.Gly638Ser)
NM_182643.3(DLC1):c.1957A>C (p.Met653Leu)
NM_182643.3(DLC1):c.1965C>T (p.Gly655=)
NM_182643.3(DLC1):c.1966C>T (p.His656Tyr)
NM_182643.3(DLC1):c.1978G>C (p.Ala660Pro)
NM_182643.3(DLC1):c.1978G>T (p.Ala660Ser)
NM_182643.3(DLC1):c.1993C>T (p.Arg665Cys)
NM_182643.3(DLC1):c.1996A>T (p.Ser666Cys)
NM_182643.3(DLC1):c.2019C>A (p.Ser673Arg)
NM_182643.3(DLC1):c.2050C>T (p.His684Tyr)
NM_182643.3(DLC1):c.2126A>G (p.Lys709Arg)
NM_182643.3(DLC1):c.2128C>G (p.Gln710Glu)
NM_182643.3(DLC1):c.2132T>G (p.Leu711Arg)
NM_182643.3(DLC1):c.2150C>A (p.Ser717Tyr)
NM_182643.3(DLC1):c.2150C>G (p.Ser717Cys)
NM_182643.3(DLC1):c.2159A>G (p.Asn720Ser)
NM_182643.3(DLC1):c.2189G>T (p.Arg730Leu)
NM_182643.3(DLC1):c.2198G>T (p.Ser733Ile)
NM_182643.3(DLC1):c.2203T>C (p.Ser735Pro)
NM_182643.3(DLC1):c.2208C>G (p.Asn736Lys)
NM_182643.3(DLC1):c.2262C>T (p.Ser754=)
NM_182643.3(DLC1):c.2279C>G (p.Thr760Arg)
NM_182643.3(DLC1):c.2314G>A (p.Val772Met)
NM_182643.3(DLC1):c.232A>G (p.Met78Val)
NM_182643.3(DLC1):c.2378A>G (p.Gln793Arg)
NM_182643.3(DLC1):c.2394C>T (p.Arg798=)
NM_182643.3(DLC1):c.2409G>C (p.Glu803Asp)
NM_182643.3(DLC1):c.2462C>T (p.Ala821Val)
NM_182643.3(DLC1):c.2471A>G (p.Asn824Ser)
NM_182643.3(DLC1):c.2490G>A (p.Ser830=)
NM_182643.3(DLC1):c.2501G>C (p.Gly834Ala)
NM_182643.3(DLC1):c.2531A>C (p.His844Pro)
NM_182643.3(DLC1):c.2540G>A (p.Gly847Asp)
NM_182643.3(DLC1):c.2548A>C (p.Ser850Arg)
NM_182643.3(DLC1):c.2557A>T (p.Arg853Trp)
NM_182643.3(DLC1):c.2576G>A (p.Ser859Asn)
NM_182643.3(DLC1):c.2612C>G (p.Ser871Cys)
NM_182643.3(DLC1):c.2630G>C (p.Ser877Thr)
NM_182643.3(DLC1):c.2644G>T (p.Val882Leu)
NM_182643.3(DLC1):c.2651G>A (p.Gly884Asp)
NM_182643.3(DLC1):c.2665T>C (p.Ser889Pro)
NM_182643.3(DLC1):c.2677G>T (p.Asp893Tyr)
NM_182643.3(DLC1):c.2719G>A (p.Asp907Asn)
NM_182643.3(DLC1):c.2725A>G (p.Ile909Val)
NM_182643.3(DLC1):c.2748G>C (p.Met916Ile)
NM_182643.3(DLC1):c.2753G>C (p.Arg918Pro) rs779524261
NM_182643.3(DLC1):c.2810T>C (p.Leu937Pro)
NM_182643.3(DLC1):c.2831C>T (p.Pro944Leu)
NM_182643.3(DLC1):c.2847_2852del (p.Gln949_Ile950del)
NM_182643.3(DLC1):c.2853C>G (p.His951Gln)
NM_182643.3(DLC1):c.2894A>G (p.Asp965Gly)
NM_182643.3(DLC1):c.2902G>A (p.Gly968Ser)
NM_182643.3(DLC1):c.2921C>T (p.Pro974Leu)
NM_182643.3(DLC1):c.292C>A (p.Leu98Ile)
NM_182643.3(DLC1):c.2941C>A (p.Pro981Thr)
NM_182643.3(DLC1):c.2990+1G>T
NM_182643.3(DLC1):c.2991-5C>A
NM_182643.3(DLC1):c.2991-5C>T
NM_182643.3(DLC1):c.299T>C (p.Leu100Pro)
NM_182643.3(DLC1):c.3021C>G (p.Ser1007Arg)
NM_182643.3(DLC1):c.3025C>T (p.His1009Tyr)
NM_182643.3(DLC1):c.3026A>G (p.His1009Arg)
NM_182643.3(DLC1):c.304G>A (p.Ala102Thr)
NM_182643.3(DLC1):c.3109C>T (p.Leu1037=)
NM_182643.3(DLC1):c.3119C>T (p.Thr1040Met)
NM_182643.3(DLC1):c.3143C>G (p.Pro1048Arg)
NM_182643.3(DLC1):c.3146C>G (p.Ser1049Cys)
NM_182643.3(DLC1):c.3150C>G (p.Asn1050Lys)
NM_182643.3(DLC1):c.3172G>A (p.Val1058Met)
NM_182643.3(DLC1):c.3217C>T (p.Arg1073Trp)
NM_182643.3(DLC1):c.3236C>T (p.Pro1079Leu)
NM_182643.3(DLC1):c.3246C>G (p.Val1082=)
NM_182643.3(DLC1):c.3263G>T (p.Gly1088Val)
NM_182643.3(DLC1):c.3283A>G (p.Ile1095Val)
NM_182643.3(DLC1):c.3313C>T (p.His1105Tyr)
NM_182643.3(DLC1):c.3327+17C>T
NM_182643.3(DLC1):c.3328-3delinsACACT
NM_182643.3(DLC1):c.3347C>A (p.Ser1116Ter)
NM_182643.3(DLC1):c.3362G>A (p.Arg1121Gln)
NM_182643.3(DLC1):c.3376C>T (p.Arg1126Cys)
NM_182643.3(DLC1):c.3389A>G (p.Glu1130Gly)
NM_182643.3(DLC1):c.3401A>G (p.Asp1134Gly)
NM_182643.3(DLC1):c.3404G>A (p.Cys1135Tyr)
NM_182643.3(DLC1):c.3414C>T (p.Tyr1138=)
NM_182643.3(DLC1):c.342T>A (p.Asp114Glu)
NM_182643.3(DLC1):c.3446T>C (p.Met1149Thr)
NM_182643.3(DLC1):c.3488C>T (p.Thr1163Met)
NM_182643.3(DLC1):c.3493A>C (p.Lys1165Gln)
NM_182643.3(DLC1):c.3500C>T (p.Ser1167Leu)
NM_182643.3(DLC1):c.3518T>C (p.Ile1173Thr)
NM_182643.3(DLC1):c.3527-12G>C
NM_182643.3(DLC1):c.3538G>A (p.Asp1180Asn)
NM_182643.3(DLC1):c.3542A>G (p.Gln1181Arg)
NM_182643.3(DLC1):c.3544C>T (p.Arg1182Cys)
NM_182643.3(DLC1):c.3545G>A (p.Arg1182His)
NM_182643.3(DLC1):c.3601C>A (p.Leu1201Met)
NM_182643.3(DLC1):c.3671A>C (p.Asn1224Thr)
NM_182643.3(DLC1):c.371A>G (p.Asp124Gly)
NM_182643.3(DLC1):c.3722G>A (p.Arg1241Lys)
NM_182643.3(DLC1):c.3740+5G>A
NM_182643.3(DLC1):c.3742G>A (p.Val1248Ile)
NM_182643.3(DLC1):c.3743T>A (p.Val1248Glu)
NM_182643.3(DLC1):c.37C>T (p.His13Tyr)
NM_182643.3(DLC1):c.3803C>T (p.Ala1268Val)
NM_182643.3(DLC1):c.3832G>T (p.Ala1278Ser)
NM_182643.3(DLC1):c.3875G>A (p.Arg1292Gln)
NM_182643.3(DLC1):c.4001A>G (p.Lys1334Arg)
NM_182643.3(DLC1):c.4025G>C (p.Gly1342Ala)
NM_182643.3(DLC1):c.4047G>A (p.Ser1349=)
NM_182643.3(DLC1):c.4073A>C (p.Lys1358Thr)
NM_182643.3(DLC1):c.4106G>A (p.Arg1369Lys)
NM_182643.3(DLC1):c.4139A>T (p.Glu1380Val)
NM_182643.3(DLC1):c.4156C>G (p.Leu1386Val)
NM_182643.3(DLC1):c.4163A>G (p.Glu1388Gly)
NM_182643.3(DLC1):c.4247A>G (p.Gln1416Arg)
NM_182643.3(DLC1):c.4250A>G (p.Asn1417Ser)
NM_182643.3(DLC1):c.4256T>C (p.Met1419Thr)
NM_182643.3(DLC1):c.4259C>G (p.Ala1420Gly)
NM_182643.3(DLC1):c.4262C>T (p.Pro1421Leu)
NM_182643.3(DLC1):c.4293-6C>A
NM_182643.3(DLC1):c.4300A>G (p.Arg1434Gly)
NM_182643.3(DLC1):c.4303A>G (p.Thr1435Ala)
NM_182643.3(DLC1):c.4313C>G (p.Pro1438Arg)
NM_182643.3(DLC1):c.4321G>A (p.Ala1441Thr)
NM_182643.3(DLC1):c.4325G>A (p.Cys1442Tyr)
NM_182643.3(DLC1):c.4351C>G (p.His1451Asp)
NM_182643.3(DLC1):c.4354G>A (p.Asp1452Asn)
NM_182643.3(DLC1):c.4358G>A (p.Arg1453His)
NM_182643.3(DLC1):c.4390C>G (p.Leu1464Val)
NM_182643.3(DLC1):c.4445A>C (p.Tyr1482Ser)
NM_182643.3(DLC1):c.4448T>C (p.Met1483Thr)
NM_182643.3(DLC1):c.4482A>C (p.Glu1494Asp)
NM_182643.3(DLC1):c.4519G>A (p.Glu1507Lys)
NM_182643.3(DLC1):c.4533C>G (p.Ile1511Met)
NM_182643.3(DLC1):c.4574C>G (p.Thr1525Ser)
NM_182643.3(DLC1):c.457A>G (p.Ile153Val)
NM_182643.3(DLC1):c.465A>G (p.Gln155=)
NM_182643.3(DLC1):c.488C>G (p.Ser163Cys)
NM_182643.3(DLC1):c.494G>T (p.Gly165Val)
NM_182643.3(DLC1):c.500C>G (p.Ala167Gly)
NM_182643.3(DLC1):c.521T>C (p.Leu174Pro)
NM_182643.3(DLC1):c.559A>G (p.Ile187Val)
NM_182643.3(DLC1):c.569G>T (p.Ser190Ile)
NM_182643.3(DLC1):c.599G>A (p.Ser200Asn)
NM_182643.3(DLC1):c.617C>T (p.Pro206Leu)
NM_182643.3(DLC1):c.620A>C (p.Lys207Thr)
NM_182643.3(DLC1):c.621A>C (p.Lys207Asn)
NM_182643.3(DLC1):c.623T>G (p.Val208Gly)
NM_182643.3(DLC1):c.631G>C (p.Val211Leu)
NM_182643.3(DLC1):c.640T>G (p.Leu214Val)
NM_182643.3(DLC1):c.646G>A (p.Val216Met)
NM_182643.3(DLC1):c.646G>T (p.Val216Leu)
NM_182643.3(DLC1):c.704G>A (p.Arg235Gln)
NM_182643.3(DLC1):c.721C>A (p.Pro241Thr)
NM_182643.3(DLC1):c.722C>A (p.Pro241His)
NM_182643.3(DLC1):c.729T>G (p.Asp243Glu)
NM_182643.3(DLC1):c.760C>T (p.Gln254Ter)
NM_182643.3(DLC1):c.792C>A (p.Asn264Lys)
NM_182643.3(DLC1):c.805T>A (p.Leu269Ile)
NM_182643.3(DLC1):c.828C>G (p.Ser276Arg)
NM_182643.3(DLC1):c.844C>T (p.Pro282Ser)
NM_182643.3(DLC1):c.874A>G (p.Asn292Asp)
NM_182643.3(DLC1):c.919C>G (p.Pro307Ala)
NM_182643.3(DLC1):c.943G>A (p.Gly315Ser)
NM_182643.3(DLC1):c.974T>C (p.Leu325Pro)
NM_182643.3(DLC1):c.974_982del (p.Leu325_Thr327del)
NM_182643.3(DLC1):c.985G>A (p.Glu329Lys)
NM_182643.3(DLC1):c.992C>G (p.Thr331Arg)

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