List of variants in gene CARD11 reported by OMIM

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.401A>G (p.Glu134Gly)	rs387907351	0.00001
CARD11, GLU57ASP
NM_032415.5(CARD11):c.2704-890_2839+352del
NM_032415.7(CARD11):c.146G>A (p.Cys49Tyr)	rs794729673
NM_032415.7(CARD11):c.2833C>T (p.Gln945Ter)	rs397514686
NM_032415.7(CARD11):c.2923C>T (p.Arg975Trp)	rs1064795307
NM_032415.7(CARD11):c.367G>A (p.Gly123Ser)	rs387907352
NM_032415.7(CARD11):c.368G>A (p.Gly123Asp)	rs571517554
NP_115791.3:p.Leu194Pro
NP_115791.3:p.Met183_Lys196dup

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