List of variants in gene CARD11 reported as likely pathogenic for immune system disorder

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.3145-3C>T	rs200456391	0.00077
NM_032415.7(CARD11):c.2921G>A (p.Arg974His)	rs750407488	0.00011
NM_032415.7(CARD11):c.2368G>A (p.Ala790Thr)	rs531252532	0.00003
NM_032415.7(CARD11):c.128C>G (p.Thr43Arg)
NM_032415.7(CARD11):c.128C>T (p.Thr43Met)	rs2115094112
NM_032415.7(CARD11):c.173A>G (p.Asp58Gly)	rs1780506565
NM_032415.7(CARD11):c.179T>A (p.Val60Glu)	rs1583410780
NM_032415.7(CARD11):c.191C>G (p.Pro64Arg)	rs1583410771
NM_032415.7(CARD11):c.1940+1G>T	rs2115046344
NM_032415.7(CARD11):c.1941-1G>T
NM_032415.7(CARD11):c.215G>T (p.Arg72Leu)	rs2115093887
NM_032415.7(CARD11):c.220+1G>A	rs1554276623
NM_032415.7(CARD11):c.223C>T (p.Arg75Trp)	rs2115090664
NM_032415.7(CARD11):c.2324C>T (p.Ser775Leu)
NM_032415.7(CARD11):c.2917C>T (p.Arg973Cys)	rs754645078
NM_032415.7(CARD11):c.358+1G>A	rs2115090359
NM_032415.7(CARD11):c.358+1_358+9delinsAACATC
NM_032415.7(CARD11):c.359-1G>A
NM_032415.7(CARD11):c.377G>A (p.Gly126Asp)	rs1423056320
NM_032415.7(CARD11):c.7+1G>C
NM_032415.7(CARD11):c.752T>C (p.Leu251Pro)	rs1780193930
NM_032415.7(CARD11):c.864+1G>A	rs1780191273
NM_032415.7(CARD11):c.864+1G>C
NM_032415.7(CARD11):c.874C>T (p.Arg292Cys)	rs771790639
NM_032415.7(CARD11):c.88C>G (p.Arg30Gly)	rs145474800

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