List of variants in gene CUBN, LOC129390143 studied for anemia

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.1245T>C (p.Gly415=)	rs12571671	0.05965
NM_001081.4(CUBN):c.1349G>A (p.Gly450Asp)	rs146463364	0.00034
NM_001081.4(CUBN):c.1358C>A (p.Ser453Tyr)	rs368630481	0.00014
NM_001081.4(CUBN):c.1236T>C (p.Thr412=)	rs201404467	0.00012
NM_001081.4(CUBN):c.1234A>G (p.Thr412Ala)	rs748933632	0.00008
NM_001081.4(CUBN):c.1351G>A (p.Val451Ile)	rs746956601	0.00003
NM_001081.4(CUBN):c.1272G>T (p.Trp424Cys)	rs563035840	0.00001
NM_001081.4(CUBN):c.1350C>T (p.Gly450=)	rs770827241	0.00001
NM_001081.4(CUBN):c.1231-10T>C
NM_001081.4(CUBN):c.1231-9T>C
NM_001081.4(CUBN):c.1231-9del
NM_001081.4(CUBN):c.1301A>G (p.Asn434Ser)
NM_001081.4(CUBN):c.1342G>A (p.Val448Ile)	rs2131301048

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