ClinVar Miner

List of variants in gene VANGL1 reported as benign for Caudal regression sequence

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP
NM_138959.3(VANGL1):c.*1043A>G rs150705915
NM_138959.3(VANGL1):c.*1277C>T rs3204955
NM_138959.3(VANGL1):c.*1627A>G rs149888685
NM_138959.3(VANGL1):c.*1652C>T
NM_138959.3(VANGL1):c.*1749G>T rs3811010
NM_138959.3(VANGL1):c.*1772A>G rs114033235
NM_138959.3(VANGL1):c.*2043C>T rs74117021
NM_138959.3(VANGL1):c.*217C>T rs41299565
NM_138959.3(VANGL1):c.*2187T>C rs146730302
NM_138959.3(VANGL1):c.*2344A>C
NM_138959.3(VANGL1):c.*2351T>G rs12121158
NM_138959.3(VANGL1):c.*2489C>T rs41299571
NM_138959.3(VANGL1):c.*2581G>A rs3811008
NM_138959.3(VANGL1):c.*25A>T
NM_138959.3(VANGL1):c.*2865A>G rs114921471
NM_138959.3(VANGL1):c.*300C>T rs41310108
NM_138959.3(VANGL1):c.*3023G>T rs10923204
NM_138959.3(VANGL1):c.*313A>G rs3811012
NM_138959.3(VANGL1):c.*3150T>C
NM_138959.3(VANGL1):c.*3336G>A rs61732170
NM_138959.3(VANGL1):c.*3409T>C
NM_138959.3(VANGL1):c.*3417C>T rs76160883
NM_138959.3(VANGL1):c.*3496T>A rs4839472
NM_138959.3(VANGL1):c.*3544C>T rs74117023
NM_138959.3(VANGL1):c.*3559G>A
NM_138959.3(VANGL1):c.*3598A>G rs187286147
NM_138959.3(VANGL1):c.*3608C>T
NM_138959.3(VANGL1):c.*3653C>T
NM_138959.3(VANGL1):c.*3742A>T
NM_138959.3(VANGL1):c.*383C>G rs75277108
NM_138959.3(VANGL1):c.*416G>A rs3811011
NM_138959.3(VANGL1):c.*4788C>G
NM_138959.3(VANGL1):c.*47G>T rs190792695
NM_138959.3(VANGL1):c.*5008T>A
NM_138959.3(VANGL1):c.*505A>G rs6700610
NM_138959.3(VANGL1):c.*5267G>A rs75064936
NM_138959.3(VANGL1):c.*5444C>G rs142497673
NM_138959.3(VANGL1):c.*5808C>T rs184708484
NM_138959.3(VANGL1):c.*6084C>G rs536289395
NM_138959.3(VANGL1):c.*694C>A rs41312690
NM_138959.3(VANGL1):c.*707C>T rs562969850
NM_138959.3(VANGL1):c.*83T>A rs3811013
NM_138959.3(VANGL1):c.*922C>T
NM_138959.3(VANGL1):c.-115G>C rs181583261
NM_138959.3(VANGL1):c.-224C>A rs191609592
NM_138959.3(VANGL1):c.-226G>C rs116216703
NM_138959.3(VANGL1):c.-239G>A
NM_138959.3(VANGL1):c.1040A>C (p.Glu347Ala) rs34059106
NM_138959.3(VANGL1):c.1050T>C (p.His350=)
NM_138959.3(VANGL1):c.1127A>G (p.Gln376Arg) rs200389969
NM_138959.3(VANGL1):c.274A>G (p.Ile92Val) rs143196463
NM_138959.3(VANGL1):c.285C>T (p.Ile95=) rs140451005
NM_138959.3(VANGL1):c.323A>G (p.Lys108Arg) rs141673853
NM_138959.3(VANGL1):c.330C>T (p.Tyr110=) rs41275546
NM_138959.3(VANGL1):c.345C>T (p.Val115=) rs79828493
NM_138959.3(VANGL1):c.346G>A (p.Ala116Thr) rs4839469
NM_138959.3(VANGL1):c.523C>T (p.Arg175Trp) rs142594314
NM_138959.3(VANGL1):c.575T>C (p.Leu192Pro) rs561312836

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