List of variants in gene CSNK2A1 reported by GenomeConnect - Simons Searchlight

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_177559.3(CSNK2A1):c.139C>G (p.Arg47Gly)	rs886041956
NM_177559.3(CSNK2A1):c.140G>A (p.Arg47Gln)	rs869312845
NM_177559.3(CSNK2A1):c.149A>C (p.Tyr50Ser)	rs869312849
NM_177559.3(CSNK2A1):c.239G>A (p.Arg80His)	rs1057518092
NM_177559.3(CSNK2A1):c.466G>T (p.Asp156Tyr)	rs1568512728
NM_177559.3(CSNK2A1):c.468T>A (p.Asp156Glu)	rs1064795110
NM_177559.3(CSNK2A1):c.593A>G (p.Lys198Arg)	rs869312840
NM_177559.3(CSNK2A1):c.934C>T (p.Arg312Trp)	rs2018124491
NM_177559.3(CSNK2A1):c.96del (p.Glu32fs)	rs1600392059

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