List of variants in gene CEBPA reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004364.5(CEBPA):c.724G>A (p.Gly242Ser)	rs530569305	0.00031
NM_004364.5(CEBPA):c.1009A>T (p.Thr337Ser)	rs587778192	0.00003
NM_004364.5(CEBPA):c.141del (p.Ala48fs)	rs137852730
NM_004364.5(CEBPA):c.147_165del (p.Glu50fs)	rs2145264004
NM_004364.5(CEBPA):c.157G>A (p.Gly53Ser)	rs1967196253
NM_004364.5(CEBPA):c.158del (p.Gly53fs)	rs2145264074
NM_004364.5(CEBPA):c.189del (p.Asp63fs)	rs2145263853
NM_004364.5(CEBPA):c.314_315insT (p.Phe106fs)	rs2145263088
NM_004364.5(CEBPA):c.442G>T (p.Glu148Ter)	rs1388478228
NM_004364.5(CEBPA):c.68del (p.Pro23fs)	rs137852728
NM_004364.5(CEBPA):c.68dup (p.His24fs)	rs137852728
NM_004364.5(CEBPA):c.932A>C (p.Gln311Pro)	rs2145258913

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