ClinVar Miner

List of variants in gene ROBO1 reported as benign for not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_002941.4(ROBO1):c.3875+4T>C rs7636043 0.96961
NM_002941.4(ROBO1):c.4282+20A>G rs9839790 0.59918
NM_002941.4(ROBO1):c.499+47311C>T rs329818 0.45684
NM_002941.4(ROBO1):c.4283-6C>T rs1027832 0.36908
NM_002941.4(ROBO1):c.1740G>A (p.Ser580=) rs2271151 0.28159
NM_002941.4(ROBO1):c.3272G>A (p.Ser1091Asn) rs35456279 0.04252
NM_002941.4(ROBO1):c.4284C>T (p.Gly1428=) rs4443127 0.03460
NM_002941.4(ROBO1):c.2973C>T (p.Ser991=) rs35926083 0.03264
NM_002941.4(ROBO1):c.2211A>T (p.Val737=) rs35446711 0.02055
NM_002941.4(ROBO1):c.4704A>C (p.Ala1568=) rs35148826 0.01541
NM_002941.4(ROBO1):c.1206C>T (p.Ser402=) rs35506479 0.01113
NM_002941.4(ROBO1):c.4599A>C (p.Glu1533Asp) rs36055689 0.01105
NM_002941.4(ROBO1):c.3373+15A>G rs116750133 0.00956
NM_002941.4(ROBO1):c.2859C>T (p.Gly953=) rs115350736 0.00945
NM_002941.4(ROBO1):c.3645A>G (p.Pro1215=) rs116125749 0.00921
NM_002941.4(ROBO1):c.3823T>C (p.Leu1275=) rs62260386 0.00658
NM_002941.4(ROBO1):c.699T>C (p.Ser233=) rs181295394 0.00605
NM_002941.4(ROBO1):c.2088+7T>G rs76931835 0.00451
NM_002941.4(ROBO1):c.499+15C>T rs188532839 0.00327
NM_002941.4(ROBO1):c.4286G>A (p.Arg1429His) rs181957931 0.00296
NM_002941.4(ROBO1):c.2765G>A (p.Arg922His) rs80104116 0.00276
NM_002941.4(ROBO1):c.2840-12G>A rs189759569 0.00248
NM_002941.4(ROBO1):c.1752T>C (p.Asn584=) rs74715114 0.00237
NM_002941.4(ROBO1):c.3246C>T (p.Asn1082=) rs34841026 0.00227
NM_002941.4(ROBO1):c.1224C>T (p.Ser408=) rs200759888 0.00226
NM_002941.4(ROBO1):c.798G>A (p.Lys266=) rs377233944 0.00225
NM_002941.4(ROBO1):c.1071C>A (p.Pro357=) rs146168228 0.00218
NM_002941.4(ROBO1):c.537C>T (p.Val179=) rs182868474 0.00196
NM_002941.4(ROBO1):c.2204G>A (p.Ser735Asn) rs34515208 0.00193
NM_002941.4(ROBO1):c.1233C>T (p.Gly411=) rs80267939 0.00141
NM_002941.4(ROBO1):c.2088+18T>C rs115284514 0.00139
NM_002941.4(ROBO1):c.159G>A (p.Ser53=) rs139237706 0.00116
NM_002941.4(ROBO1):c.3102G>A (p.Glu1034=) rs180987734 0.00096
NM_002941.4(ROBO1):c.1356G>A (p.Arg452=) rs373082633 0.00062
NM_002941.4(ROBO1):c.3563C>T (p.Pro1188Leu) rs199946327 0.00056
NM_002941.4(ROBO1):c.1776A>G (p.Thr592=) rs374858268 0.00045
NM_002941.4(ROBO1):c.88+7G>T rs138253452 0.00036
NM_002941.4(ROBO1):c.2615-10G>A rs376272469 0.00027
NM_002941.4(ROBO1):c.1155G>A (p.Arg385=) rs532851420 0.00025
NM_002941.4(ROBO1):c.2154C>T (p.His718=) rs370661806 0.00015
NM_002941.4(ROBO1):c.372T>C (p.Ser124=) rs575315994 0.00010
NM_002941.4(ROBO1):c.4608T>C (p.Asp1536=) rs369610856 0.00010
NM_002941.4(ROBO1):c.88+12G>A rs544718083 0.00010
NM_002941.4(ROBO1):c.3411A>G (p.Pro1137=) rs568106352 0.00005
NM_002941.4(ROBO1):c.3811C>T (p.Leu1271Phe) rs117415292 0.00005
NM_002941.4(ROBO1):c.4800T>G (p.Asp1600Glu) rs748131500 0.00005
NM_002941.4(ROBO1):c.121G>C (p.Gly41Arg) rs200733765
NM_002941.4(ROBO1):c.1342+19del rs1330539749
NM_002941.4(ROBO1):c.2793C>A (p.Thr931=) rs6795556
NM_002941.4(ROBO1):c.2840-14del rs763576136
NM_002941.4(ROBO1):c.2840-14dup rs763576136
NM_002941.4(ROBO1):c.2883-7del rs369027577
NM_002941.4(ROBO1):c.2883-7dup rs369027577
NM_002941.4(ROBO1):c.4360G>T (p.Val1454Leu) rs200590399
NM_002941.4(ROBO1):c.658-4dup rs750375001

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