ClinVar Miner

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

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Total variants: 9
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HGVS dbSNP
NM_018055.4(NODAL):c.*356G>A rs556853359
NM_018055.4(NODAL):c.*404T>C rs77232076
NM_018055.4(NODAL):c.*479C>T rs80138796
NM_018055.4(NODAL):c.*62A>T rs76889088
NM_018055.4(NODAL):c.*886G>A rs58468830
NM_018055.4(NODAL):c.216C>T (p.Asn72=) rs138195571
NM_018055.4(NODAL):c.357C>T (p.Pro119=) rs77151171
NM_018055.4(NODAL):c.588C>G (p.Leu196=) rs2231959
NM_018055.4(NODAL):c.607G>A (p.Glu203Lys) rs10999334

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