List of variants in gene CSNK2A1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_177559.3(CSNK2A1):c.997C>T (p.Arg333Ter)	rs2018100989	0.00001
GRCh37/hg19 20p13(chr20:478365-480578)x1
NM_177559.3(CSNK2A1):c.1025dup (p.Ser343fs)
NM_177559.3(CSNK2A1):c.149A>G (p.Tyr50Cys)	rs869312849
NM_177559.3(CSNK2A1):c.239G>A (p.Arg80His)	rs1057518092
NM_177559.3(CSNK2A1):c.242A>C (p.Glu81Ala)
NM_177559.3(CSNK2A1):c.327dup (p.Ala110fs)	rs2018409484
NM_177559.3(CSNK2A1):c.468T>A (p.Asp156Glu)	rs1064795110
NM_177559.3(CSNK2A1):c.473A>G (p.Lys158Arg)	rs2122531973
NM_177559.3(CSNK2A1):c.52_55del (p.His18fs)
NM_177559.3(CSNK2A1):c.530G>A (p.Gly177Asp)	rs2122521881
NM_177559.3(CSNK2A1):c.583C>T (p.Arg195Ter)	rs1034583315
NM_177559.3(CSNK2A1):c.71G>A (p.Trp24Ter)	rs2018650698
NM_177559.3(CSNK2A1):c.723+1G>C	rs2018178212
NM_177559.3(CSNK2A1):c.832C>T (p.Arg278Ter)	rs2018126184
NM_177559.3(CSNK2A1):c.916C>T (p.Arg306Ter)	rs1380843831
NM_177559.3(CSNK2A1):c.921T>G (p.Tyr307Ter)	rs760778054
NM_177559.3(CSNK2A1):c.935G>A (p.Arg312Gln)	rs2122506319

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