ClinVar Miner

List of variants in gene NODAL reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_018055.5(NODAL):c.494A>G (p.His165Arg) rs1904589 0.56006
NM_018055.5(NODAL):c.193+12C>T rs10999338 0.35409
NM_018055.5(NODAL):c.588C>G (p.Leu196=) rs2231959 0.00714
NM_018055.5(NODAL):c.916C>T (p.His306Tyr) rs148708629 0.00085
NM_018055.5(NODAL):c.904C>T (p.Arg302Cys) rs150819707 0.00051
NM_018055.5(NODAL):c.531T>C (p.Ala177=) rs145468639 0.00016
NM_018055.5(NODAL):c.607G>A (p.Glu203Lys) rs10999334 0.00015
NM_018055.5(NODAL):c.281G>A (p.Arg94Gln) rs146018217 0.00007
NM_018055.5(NODAL):c.778G>A (p.Gly260Arg) rs121909283 0.00004
NM_018055.5(NODAL):c.963G>A (p.Leu321=) rs772060498 0.00001
NM_018055.5(NODAL):c.222G>A (p.Thr74=)
NM_018055.5(NODAL):c.329C>T (p.Ala110Val)
NM_018055.5(NODAL):c.502G>T (p.Ala168Ser)
NM_018055.5(NODAL):c.700_723delinsTTGACTTCC (p.Arg234_Pro241delinsLeuThrSer) rs2132214841
NM_018055.5(NODAL):c.835G>A (p.Glu279Lys)
NM_018055.5(NODAL):c.945A>G (p.Pro315=) rs1589151449

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