List of variants in gene BNC2 reported by Centre for molecular medicine, Karolinska Institutet

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_017637.6(BNC2):c.1545A>G (p.Ser515=)	rs117470554	0.04304
NM_017637.6(BNC2):c.84A>T (p.Ala28=)	rs76485966	0.02974
NM_017637.6(BNC2):c.2768C>T (p.Ala923Val)	rs117452684	0.01981
NM_017637.6(BNC2):c.936C>T (p.Phe312=)	rs77464990	0.01212
NM_017637.6(BNC2):c.2920A>G (p.Ile974Val)	rs35005898	0.00945
NM_017637.6(BNC2):c.1240C>G (p.Leu414Val)	rs148873573	0.00784
NM_017637.6(BNC2):c.2789A>G (p.Asp930Gly)	rs41268965	0.00269
NM_017637.6(BNC2):c.519C>T (p.Ser173=)	rs149019822	0.00149
NM_017637.6(BNC2):c.171G>T (p.Gln57His)	rs145011045	0.00058
NM_017637.6(BNC2):c.501C>T (p.Val167=)	rs143821778	0.00002
NM_017637.6(BNC2):c.1239T>C (p.Asp413=)	rs483353011	0.00001
NM_017637.6(BNC2):c.1002A>G (p.Pro334=)	rs483353010
NM_017637.6(BNC2):c.2739C>T (p.Arg913=)	rs189895388
NM_017637.6(BNC2):c.916C>G (p.Pro306Ala)	rs114964332

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