ClinVar Miner

List of variants in gene ROBO3 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_022370.4(ROBO3):c.-60G>T rs543770866 0.00180
NM_022370.4(ROBO3):c.2993G>T (p.Gly998Val) rs75098003 0.00167
NM_022370.4(ROBO3):c.3921C>T (p.Ala1307=) rs374359013 0.00106
NM_022370.4(ROBO3):c.3525G>A (p.Gln1175=) rs199650068 0.00105
NM_022370.4(ROBO3):c.769C>T (p.Arg257Cys) rs200451819 0.00105
NM_022370.4(ROBO3):c.2308G>T (p.Gly770Cys) rs201976275 0.00084
NM_022370.4(ROBO3):c.2310C>T (p.Gly770=) rs200678379 0.00084
NM_022370.4(ROBO3):c.*68C>G rs886047914 0.00073
NM_022370.4(ROBO3):c.2020C>T (p.Arg674Cys) rs201405429 0.00073
NM_022370.4(ROBO3):c.3567T>C (p.Ser1189=) rs201358102 0.00071
NM_022370.4(ROBO3):c.3780G>A (p.Arg1260=) rs369974414 0.00040
NM_022370.4(ROBO3):c.1194G>A (p.Thr398=) rs369032140 0.00035
NM_022370.4(ROBO3):c.2183G>A (p.Ser728Asn) rs189303564 0.00019
NM_022370.4(ROBO3):c.2048C>T (p.Pro683Leu) rs778522624 0.00013
NM_022370.4(ROBO3):c.3836C>T (p.Ala1279Val) rs201702041 0.00013
NM_022370.4(ROBO3):c.2061G>C (p.Gln687His) rs370172611 0.00012
NM_022370.4(ROBO3):c.592G>A (p.Val198Met) rs192622083 0.00011
NM_022370.4(ROBO3):c.1619-9C>T rs369359848 0.00010
NM_022370.4(ROBO3):c.1634C>T (p.Ser545Leu) rs755519737 0.00006
NM_022370.4(ROBO3):c.2879C>T (p.Ser960Leu) rs539782442 0.00006
NM_022370.4(ROBO3):c.3922G>A (p.Val1308Met) rs752717878 0.00006
NM_022370.4(ROBO3):c.630G>A (p.Glu210=) rs745923389 0.00006
NM_022370.4(ROBO3):c.2102G>T (p.Gly701Val) rs184921255 0.00005
NM_022370.4(ROBO3):c.4010G>A (p.Gly1337Asp) rs770384513 0.00005
NM_022370.4(ROBO3):c.4098T>C (p.Ser1366=) rs55725290 0.00005
NM_022370.4(ROBO3):c.770G>A (p.Arg257His) rs750349831 0.00004
NM_022370.4(ROBO3):c.1752T>G (p.Ala584=) rs778743655 0.00003
NM_022370.4(ROBO3):c.2699C>T (p.Ala900Val) rs746827802 0.00003
NM_022370.4(ROBO3):c.3275G>C (p.Cys1092Ser) rs771199444 0.00003
NM_022370.4(ROBO3):c.3354T>A (p.Pro1118=) rs751291981 0.00003
NM_022370.4(ROBO3):c.3462C>T (p.Ala1154=) rs375010463 0.00003
NM_022370.4(ROBO3):c.3886C>G (p.Arg1296Gly) rs575251327 0.00003
NM_022370.4(ROBO3):c.43T>C (p.Phe15Leu) rs774646580 0.00003
NM_022370.4(ROBO3):c.716C>T (p.Ser239Phe) rs765531515 0.00003
NM_022370.4(ROBO3):c.*91C>A rs965189500 0.00002
NM_022370.4(ROBO3):c.1379A>G (p.Gln460Arg) rs771613910 0.00002
NM_022370.4(ROBO3):c.1805G>T (p.Trp602Leu) rs772421418 0.00002
NM_022370.4(ROBO3):c.2007G>A (p.Ala669=) rs753075502 0.00002
NM_022370.4(ROBO3):c.2947T>C (p.Cys983Arg) rs765206958 0.00002
NM_022370.4(ROBO3):c.3042C>T (p.Gly1014=) rs568538420 0.00002
NM_022370.4(ROBO3):c.3372G>A (p.Thr1124=) rs756071747 0.00002
NM_022370.4(ROBO3):c.4087C>T (p.Arg1363Trp) rs561165246 0.00002
NM_022370.4(ROBO3):c.4100G>A (p.Arg1367Gln) rs200255001 0.00002
NM_022370.4(ROBO3):c.637A>C (p.Arg213=) rs373366899 0.00002
NM_022370.4(ROBO3):c.1617G>A (p.Arg539=) rs199609085 0.00001
NM_022370.4(ROBO3):c.1808G>A (p.Arg603His) rs775868268 0.00001
NM_022370.4(ROBO3):c.2779+9C>T rs756785207 0.00001
NM_022370.4(ROBO3):c.3320+12C>T rs761311616 0.00001
NM_022370.4(ROBO3):c.3350T>C (p.Met1117Thr) rs765934190 0.00001
NM_022370.4(ROBO3):c.646-11T>G rs778092268 0.00001
NM_022370.4(ROBO3):c.733C>T (p.Arg245Trp) rs121918277 0.00001
NM_022370.4(ROBO3):c.*111C>T rs886047915
NM_022370.4(ROBO3):c.*151CTTT[2] rs886047916
NM_022370.4(ROBO3):c.*64C>G rs761468358
NM_022370.4(ROBO3):c.*67C>G rs189881000
NM_022370.4(ROBO3):c.*67C>T rs189881000
NM_022370.4(ROBO3):c.1034-13C>G rs886047908
NM_022370.4(ROBO3):c.1189C>T (p.Pro397Ser) rs114572753
NM_022370.4(ROBO3):c.1515C>T (p.Thr505=) rs769591533
NM_022370.4(ROBO3):c.1953T>C (p.Asp651=) rs1157938168
NM_022370.4(ROBO3):c.1957A>C (p.Ser653Arg) rs550454340
NM_022370.4(ROBO3):c.2329dup (p.Val777fs) rs750231138
NM_022370.4(ROBO3):c.2931A>T (p.Glu977Asp) rs763859563
NM_022370.4(ROBO3):c.3091A>C (p.Thr1031Pro) rs886047909
NM_022370.4(ROBO3):c.3139T>G (p.Trp1047Gly) rs886047910
NM_022370.4(ROBO3):c.3300G>C (p.Pro1100=) rs550792725
NM_022370.4(ROBO3):c.3551C>A (p.Pro1184Gln) rs368839094
NM_022370.4(ROBO3):c.3706G>A (p.Gly1236Arg) rs886047912
NM_022370.4(ROBO3):c.3707G>T (p.Gly1236Val) rs886047913
NM_022370.4(ROBO3):c.3788G>C (p.Ser1263Thr) rs1946505879
NM_022370.4(ROBO3):c.4137_4138del (p.Lys1380fs) rs1277832845
NM_022370.4(ROBO3):c.468C>T (p.Asn156=) rs766578334
NM_022370.4(ROBO3):c.571dup (p.Arg191fs) rs756837590
NM_022370.4(ROBO3):c.764T>C (p.Leu255Pro) rs747047729

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