List of variants in gene CSNK2B studied for CSNK2B-related disorder

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001320.7(CSNK2B):c.-1G>C	rs144133926	0.00066
NM_001320.7(CSNK2B):c.252C>T (p.His84=)	rs761163913	0.00002
NM_001320.7(CSNK2B):c.292T>C (p.Leu98=)	rs571224228	0.00001
NM_001320.7(CSNK2B):c.139C>T (p.Arg47Ter)	rs1085307703
NM_001320.7(CSNK2B):c.175+1G>A	rs2536958403
NM_001320.7(CSNK2B):c.462G>A (p.Thr154=)	rs143237802
NM_001320.7(CSNK2B):c.505A>G (p.Met169Val)	rs2536968227
NM_001320.7(CSNK2B):c.558-2A>C
NM_001320.7(CSNK2B):c.639G>A (p.Thr213=)	rs144120994
NM_001320.7(CSNK2B):c.6C>T (p.Ser2=)	rs1801756577
NM_001320.7(CSNK2B):c.70G>T (p.Glu24Ter)	rs2151182211
NM_001320.7(CSNK2B):c.94G>A (p.Asp32Asn)	rs1554169984

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