List of variants in gene CUBN, LOC126860871 studied for inborn disorder of amino acid metabolism

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.594-34G>A	rs2295813	0.91875
NM_001081.4(CUBN):c.618C>T (p.Tyr206=)	rs41289313	0.06126
NM_001081.4(CUBN):c.671G>A (p.Arg224His)	rs139891639	0.00041
NM_001081.4(CUBN):c.614C>T (p.Thr205Met)	rs374652141	0.00009
NM_001081.4(CUBN):c.703C>T (p.Arg235Ter)	rs1461982823	0.00001
NM_001081.4(CUBN):c.626A>G (p.Gln209Arg)
NM_001081.4(CUBN):c.670C>T (p.Arg224Cys)
NM_001081.4(CUBN):c.702G>T (p.Met234Ile)
NM_001081.4(CUBN):c.704G>A (p.Arg235Gln)

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