ClinVar Miner

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

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Total variants: 15
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HGVS dbSNP
NM_138959.3(VANGL1):c.*1545A>G rs117337677
NM_138959.3(VANGL1):c.*2336A>G rs148944333
NM_138959.3(VANGL1):c.*5466G>A rs192325588
NM_138959.3(VANGL1):c.1023C>T (p.Asn341=)
NM_138959.3(VANGL1):c.114C>T (p.Asp38=) rs201840785
NM_138959.3(VANGL1):c.1172G>T (p.Arg391Met) rs140485834
NM_138959.3(VANGL1):c.1299C>T (p.Asn433=)
NM_138959.3(VANGL1):c.231G>A (p.Thr77=) rs186509771
NM_138959.3(VANGL1):c.435T>C (p.Cys145=) rs34768472
NM_138959.3(VANGL1):c.51G>A (p.Ser17=)
NM_138959.3(VANGL1):c.572T>C (p.Val191Ala) rs781010619
NM_138959.3(VANGL1):c.73G>A (p.Glu25Lys)
NM_138959.3(VANGL1):c.812+9C>T rs370321176
NM_138959.3(VANGL1):c.868T>C (p.Tyr290His)
NM_138959.3(VANGL1):c.98C>T (p.Ser33Leu)

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