List of variants in gene CSNK2B studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001320.7(CSNK2B):c.107T>C (p.Leu36Pro)	rs2151185393
NM_001320.7(CSNK2B):c.116T>C (p.Leu39Pro)	rs2151185431
NM_001320.7(CSNK2B):c.124C>T (p.Gln42Ter)	rs1339457069
NM_001320.7(CSNK2B):c.139C>T (p.Arg47Ter)	rs1085307703
NM_001320.7(CSNK2B):c.238T>A (p.Tyr80Asn)	rs1554170318
NM_001320.7(CSNK2B):c.245T>A (p.Leu82Ter)	rs1801960712
NM_001320.7(CSNK2B):c.256C>T (p.Arg86Cys)	rs1801961640
NM_001320.7(CSNK2B):c.291+2T>C
NM_001320.7(CSNK2B):c.367+3_367+5delinsAAA
NM_001320.7(CSNK2B):c.446C>G (p.Ser149Ter)	rs2536967921
NM_001320.7(CSNK2B):c.464_467del (p.Asp155fs)	rs2536968042
NM_001320.7(CSNK2B):c.491C>T (p.Pro164Leu)	rs2151188947
NM_001320.7(CSNK2B):c.495_496del (p.Met166fs)	rs2151188957
NM_001320.7(CSNK2B):c.566G>T (p.Gly189Val)	rs1802055915
NM_001320.7(CSNK2B):c.67T>C (p.Cys23Arg)	rs2536947987
NM_001320.7(CSNK2B):c.72+1G>A	rs1801761541
NM_001320.7(CSNK2B):c.73-2A>G	rs1554169967
NM_001320.7(CSNK2B):c.94G>A (p.Asp32Asn)	rs1554169984

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