ClinVar Miner

List of variants reported as likely benign for vesicoureteral reflux by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_001365276.2(TNXB):c.10607-19C>A rs773540524 0.01008
NM_001365276.2(TNXB):c.113G>A (p.Arg38Gln) rs149502087 0.00876
NM_001365276.2(TNXB):c.4484C>T (p.Thr1495Ile) rs6910390 0.00842
NM_001365276.2(TNXB):c.2385A>G (p.Thr795=) rs185461070 0.00300
NM_001365276.2(TNXB):c.12058+15G>A rs762839811 0.00275
NM_001395656.1(ROBO2):c.2742T>C (p.Arg914=) rs183858273 0.00255
NM_001365276.2(TNXB):c.12592G>A (p.Ala4198Thr) rs756508366 0.00233
NM_022454.4(SOX17):c.585G>T (p.Leu195=) rs371736816 0.00214
NM_001395656.1(ROBO2):c.1956T>C (p.Thr652=) rs61731263 0.00179
NM_001395656.1(ROBO2):c.462C>T (p.Cys154=) rs200353960 0.00099
NM_001395656.1(ROBO2):c.471C>T (p.Pro157=) rs201406456 0.00089
NM_001365276.2(TNXB):c.10713C>T (p.Ser3571=) rs758424441 0.00072
NM_001395656.1(ROBO2):c.4323C>T (p.Thr1441=) rs201527229 0.00063
NM_001365276.2(TNXB):c.7802C>T (p.Pro2601Leu) rs575866552 0.00053
NM_001365276.2(TNXB):c.4209C>T (p.Thr1403=) rs148934769 0.00047
NM_001365276.2(TNXB):c.9762C>T (p.Pro3254=) rs190855421 0.00047
NM_001365276.2(TNXB):c.8468-1G>A rs200718357 0.00039
NM_001395656.1(ROBO2):c.3888G>A (p.Lys1296=) rs200933374 0.00027
NM_001365276.2(TNXB):c.12058+6T>G rs761600175 0.00022
NM_001365276.2(TNXB):c.7413T>C (p.Pro2471=) rs375764263 0.00016
NM_001365276.2(TNXB):c.7417C>T (p.Arg2473Cys) rs373029180 0.00014
NM_001365276.2(TNXB):c.6303A>G (p.Leu2101=) rs761030884 0.00012
NM_001365276.2(TNXB):c.12210+5G>A rs4959085 0.00011
NM_001395656.1(ROBO2):c.1296G>T (p.Thr432=) rs191732065 0.00011
NM_001395656.1(ROBO2):c.204G>A (p.Gly68=) rs201531318 0.00010
NM_001395656.1(ROBO2):c.3765T>C (p.Ser1255=) rs201292837 0.00009
NM_001395656.1(ROBO2):c.1169C>T (p.Ala390Val) rs199705591 0.00006
NM_022454.4(SOX17):c.549C>T (p.Phe183=) rs929689090 0.00005
NM_022454.4(SOX17):c.948A>G (p.Gln316=) rs888660919 0.00005
NM_001395656.1(ROBO2):c.171G>T (p.Arg57=) rs752240818 0.00004
NM_001395656.1(ROBO2):c.1861+15T>C rs770007839 0.00004
NM_001395656.1(ROBO2):c.2738+9C>T rs573265362 0.00004
NM_001395656.1(ROBO2):c.4293T>G (p.Ser1431=) rs758687620 0.00004
NM_022454.4(SOX17):c.654G>A (p.Pro218=) rs770677973 0.00001
NM_001365276.2(TNXB):c.12156C>G (p.Arg4052=) rs6457479
NM_001365276.2(TNXB):c.5442C>G (p.Asp1814Glu) rs181025235
NM_001395656.1(ROBO2):c.1448G>A (p.Arg483Gln)
NM_001395656.1(ROBO2):c.1596G>A (p.Pro532=) rs779025170
NM_001395656.1(ROBO2):c.1964C>T (p.Thr655Met)
NM_001395656.1(ROBO2):c.3241C>G (p.Pro1081Ala)
NM_001395656.1(ROBO2):c.3243C>G (p.Pro1081=) rs377172589
NM_001395656.1(ROBO2):c.3245C>G (p.Pro1082Arg) rs374166639
NM_001395656.1(ROBO2):c.3245dup (p.Val1083fs)
NM_001395656.1(ROBO2):c.3466A>G (p.Thr1156Ala)
NM_001395656.1(ROBO2):c.3866C>T (p.Pro1289Leu)
NM_022454.4(SOX17):c.532G>T (p.Gly178Cys) rs267607082
NM_022454.4(SOX17):c.704C>A (p.Ala235Asp)
NM_022454.4(SOX17):c.911G>A (p.Gly304Glu)

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