ClinVar Miner

List of variants reported as uncertain significance for Caudal regression sequence

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ClinVar version:
Total variants: 91
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HGVS dbSNP
NM_138959.3(VANGL1):c.*1042C>A rs886045125
NM_138959.3(VANGL1):c.*1402C>G
NM_138959.3(VANGL1):c.*1456T>C rs886045126
NM_138959.3(VANGL1):c.*1483C>T rs886045127
NM_138959.3(VANGL1):c.*1492G>A
NM_138959.3(VANGL1):c.*1492G>T
NM_138959.3(VANGL1):c.*1516A>C rs886045128
NM_138959.3(VANGL1):c.*1638A>G
NM_138959.3(VANGL1):c.*1748C>T
NM_138959.3(VANGL1):c.*1749G>A rs3811010
NM_138959.3(VANGL1):c.*1970C>A rs746455152
NM_138959.3(VANGL1):c.*2009C>T
NM_138959.3(VANGL1):c.*2099G>T rs886045129
NM_138959.3(VANGL1):c.*2107A>G rs886045130
NM_138959.3(VANGL1):c.*2116A>T rs886045131
NM_138959.3(VANGL1):c.*229T>A
NM_138959.3(VANGL1):c.*2329C>T rs188964296
NM_138959.3(VANGL1):c.*234A>G
NM_138959.3(VANGL1):c.*2460C>T rs886045132
NM_138959.3(VANGL1):c.*2504A>G
NM_138959.3(VANGL1):c.*2541G>A rs886045133
NM_138959.3(VANGL1):c.*2542C>T rs886045134
NM_138959.3(VANGL1):c.*2592T>C
NM_138959.3(VANGL1):c.*2695C>A rs540290490
NM_138959.3(VANGL1):c.*2708G>A
NM_138959.3(VANGL1):c.*2917G>A
NM_138959.3(VANGL1):c.*2961T>G
NM_138959.3(VANGL1):c.*2992G>A rs886045135
NM_138959.3(VANGL1):c.*301G>C rs193075321
NM_138959.3(VANGL1):c.*3049G>C
NM_138959.3(VANGL1):c.*3123A>G rs143712039
NM_138959.3(VANGL1):c.*3267C>T
NM_138959.3(VANGL1):c.*3273A>G
NM_138959.3(VANGL1):c.*3289A>G rs886045136
NM_138959.3(VANGL1):c.*3290A>G
NM_138959.3(VANGL1):c.*340C>G rs886045121
NM_138959.3(VANGL1):c.*3666G>A rs886045138
NM_138959.3(VANGL1):c.*3671T>C
NM_138959.3(VANGL1):c.*3708C>T
NM_138959.3(VANGL1):c.*3720T>C rs886045139
NM_138959.3(VANGL1):c.*3844A>G
NM_138959.3(VANGL1):c.*4041T>C
NM_138959.3(VANGL1):c.*4209A>G
NM_138959.3(VANGL1):c.*4254A>G
NM_138959.3(VANGL1):c.*4272T>G
NM_138959.3(VANGL1):c.*4347C>T
NM_138959.3(VANGL1):c.*4463A>G rs886045142
NM_138959.3(VANGL1):c.*4676C>G rs886045143
NM_138959.3(VANGL1):c.*4800C>A
NM_138959.3(VANGL1):c.*483A>G rs886045122
NM_138959.3(VANGL1):c.*4846G>C rs868558700
NM_138959.3(VANGL1):c.*5022T>G rs886045145
NM_138959.3(VANGL1):c.*5036G>A
NM_138959.3(VANGL1):c.*5066C>G rs751663783
NM_138959.3(VANGL1):c.*5132G>T rs549041171
NM_138959.3(VANGL1):c.*5267G>T rs75064936
NM_138959.3(VANGL1):c.*5351G>A rs762453158
NM_138959.3(VANGL1):c.*5413A>C rs886045146
NM_138959.3(VANGL1):c.*5862G>A rs868196412
NM_138959.3(VANGL1):c.*5929G>A rs886045149
NM_138959.3(VANGL1):c.*5993C>G rs886045150
NM_138959.3(VANGL1):c.*6128T>C rs181588954
NM_138959.3(VANGL1):c.*634T>C rs546423374
NM_138959.3(VANGL1):c.*6360C>T rs886045151
NM_138959.3(VANGL1):c.*6474T>G rs886045152
NM_138959.3(VANGL1):c.*6602C>T rs886045153
NM_138959.3(VANGL1):c.*6640G>A rs746958675
NM_138959.3(VANGL1):c.*6681A>G
NM_138959.3(VANGL1):c.*6687A>G
NM_138959.3(VANGL1):c.*6794C>A
NM_138959.3(VANGL1):c.*6837A>G
NM_138959.3(VANGL1):c.*758G>A rs546932643
NM_138959.3(VANGL1):c.*801A>C
NM_138959.3(VANGL1):c.*929G>A rs886045123
NM_138959.3(VANGL1):c.-145G>T rs559438343
NM_138959.3(VANGL1):c.-171C>A rs886045117
NM_138959.3(VANGL1):c.1201A>C (p.Met401Leu)
NM_138959.3(VANGL1):c.1210G>T (p.Ala404Ser)
NM_138959.3(VANGL1):c.1491T>G (p.Ile497Met)
NM_138959.3(VANGL1):c.1529A>G (p.Lys510Arg)
NM_138959.3(VANGL1):c.312G>C (p.Gly104=)
NM_138959.3(VANGL1):c.316G>A (p.Asp106Asn) rs867892644
NM_138959.3(VANGL1):c.453G>A (p.Gly151=)
NM_138959.3(VANGL1):c.542G>A (p.Arg181Gln) rs761123443
NM_138959.3(VANGL1):c.612C>T (p.Tyr204=)
NM_138959.3(VANGL1):c.619C>T (p.Arg207Cys)
NM_138959.3(VANGL1):c.681G>A (p.Val227=)
NM_138959.3(VANGL1):c.759G>C (p.Gln253His)
NM_138959.3(VANGL1):c.765C>T (p.Val255=) rs368722418
NM_138959.3(VANGL1):c.867C>A (p.Ile289=)
NM_138959.3(VANGL1):c.914A>T (p.His305Leu) rs886045119

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