List of variants in gene CARD14 reported by Yale Center for Mendelian Genomics, Yale University

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_001366385.1(CARD14):c.349G>A (p.Gly117Ser)	rs281875215	0.00001
NM_001366385.1(CARD14):c.349+5G>C	rs587777763
NM_001366385.1(CARD14):c.356T>C (p.Met119Thr)	rs1598639584
NM_001366385.1(CARD14):c.356T>G (p.Met119Arg)	rs1598639584
NM_001366385.1(CARD14):c.371T>C (p.Leu124Pro)	rs1598639617
NM_001366385.1(CARD14):c.380G>C (p.Cys127Ser)	rs1598639659
NM_001366385.1(CARD14):c.412G>A (p.Glu138Lys)	rs1567872320
NM_001366385.1(CARD14):c.467T>C (p.Leu156Pro)	rs387907240
NM_001366385.1(CARD14):c.470A>C (p.Gln157Pro)	rs1598639974

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