ClinVar Miner

List of variants in gene NODAL reported as likely benign for Holoprosencephaly sequence

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Total variants: 6
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HGVS dbSNP
NM_018055.5(NODAL):c.*677C>T rs184218697
NM_018055.5(NODAL):c.281G>A (p.Arg94Gln) rs146018217
NM_018055.5(NODAL):c.417C>T (p.Val139=) rs764201898
NM_018055.5(NODAL):c.607G>A (p.Glu203Lys) rs10999334
NM_018055.5(NODAL):c.904C>T (p.Arg302Cys) rs150819707
NM_018055.5(NODAL):c.963G>A (p.Leu321=) rs772060498

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