ClinVar Miner

List of variants reported as uncertain significance for Vesicoureteral reflux 2 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 61
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HGVS dbSNP
NM_001128929.3(ROBO2):c.*1013C>T rs886058880
NM_001128929.3(ROBO2):c.*1075T>C rs886058881
NM_001128929.3(ROBO2):c.*1435C>A rs886058882
NM_001128929.3(ROBO2):c.*1488T>G
NM_001128929.3(ROBO2):c.*1516G>A rs886058883
NM_001128929.3(ROBO2):c.*1579A>G rs886058884
NM_001128929.3(ROBO2):c.*166T>C rs886058878
NM_001128929.3(ROBO2):c.*178C>G
NM_001128929.3(ROBO2):c.*1888C>T rs886058886
NM_001128929.3(ROBO2):c.*1890G>A
NM_001128929.3(ROBO2):c.*1894A>G rs886058887
NM_001128929.3(ROBO2):c.*1915C>T rs886058888
NM_001128929.3(ROBO2):c.*1950T>G rs543178648
NM_001128929.3(ROBO2):c.*2104A>G rs757318528
NM_001128929.3(ROBO2):c.*2195C>T rs372439657
NM_001128929.3(ROBO2):c.*2370C>T rs886058889
NM_001128929.3(ROBO2):c.*2591G>T
NM_001128929.3(ROBO2):c.*2679G>A
NM_001128929.3(ROBO2):c.*2886A>C rs886058891
NM_001128929.3(ROBO2):c.*2921C>T
NM_001128929.3(ROBO2):c.*3276T>C rs886058892
NM_001128929.3(ROBO2):c.*3313T>C rs538973204
NM_001128929.3(ROBO2):c.*3363T>G
NM_001128929.3(ROBO2):c.*3516T>C
NM_001128929.3(ROBO2):c.*3536G>A rs886058894
NM_001128929.3(ROBO2):c.*3594T>A
NM_001128929.3(ROBO2):c.*3707G>A
NM_001128929.3(ROBO2):c.*3804T>C
NM_001128929.3(ROBO2):c.*3809A>C rs886058896
NM_001128929.3(ROBO2):c.*3894A>G rs886058897
NM_001128929.3(ROBO2):c.*850A>G
NM_001128929.3(ROBO2):c.*913A>G
NM_001128929.3(ROBO2):c.*947C>T rs550745516
NM_001128929.3(ROBO2):c.*972T>C rs886058879
NM_001128929.3(ROBO2):c.*985C>T rs114687906
NM_001128929.3(ROBO2):c.110-57338C>G rs542668375
NM_001128929.3(ROBO2):c.110-57394C>T rs886058875
NM_001128929.3(ROBO2):c.110-57710C>T rs886058874
NM_001128929.3(ROBO2):c.110-57790A>G rs886058873
NM_001128929.3(ROBO2):c.110-57799C>G rs886058872
NM_001128929.3(ROBO2):c.1311A>G (p.Leu437=)
NM_001128929.3(ROBO2):c.1313A>G (p.Gln438Arg)
NM_001128929.3(ROBO2):c.1470G>A (p.Gln490=)
NM_001128929.3(ROBO2):c.1695C>G (p.Thr565=)
NM_001128929.3(ROBO2):c.1702G>A (p.Ala568Thr)
NM_001128929.3(ROBO2):c.1881T>C (p.Asp627=) rs757943652
NM_001128929.3(ROBO2):c.2055A>C (p.Arg685=) rs886058877
NM_001128929.3(ROBO2):c.2060T>C (p.Met687Thr)
NM_001128929.3(ROBO2):c.2092T>C (p.Ser698Pro)
NM_001128929.3(ROBO2):c.2236C>T (p.Arg746Cys)
NM_001128929.3(ROBO2):c.266C>G (p.Thr89Ser)
NM_001128929.3(ROBO2):c.3333A>G (p.Gln1111=)
NM_001128929.3(ROBO2):c.3821C>T (p.Thr1274Ile) rs772069288
NM_001128929.3(ROBO2):c.387G>T (p.Arg129Ser)
NM_001128929.3(ROBO2):c.4025C>G (p.Pro1342Arg)
NM_001128929.3(ROBO2):c.4112G>A (p.Arg1371His) rs771581041
NM_001128929.3(ROBO2):c.420G>A (p.Ala140=)
NM_001128929.3(ROBO2):c.515C>T (p.Pro172Leu)
NM_001128929.3(ROBO2):c.606A>G (p.Gly202=) rs886058876
NM_001128929.3(ROBO2):c.676G>A (p.Gly226Arg)
NM_001128929.3(ROBO2):c.823A>G (p.Lys275Glu)

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