List of variants in gene CARD11 reported as not provided by ITMI

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.1590A>C (p.Glu530Asp)	rs41515445	0.02483
NM_032415.7(CARD11):c.1630A>C (p.Ile544Leu)	rs147687933	0.00276
NM_032415.7(CARD11):c.1610G>C (p.Ser537Thr)	rs148753096	0.00226
NM_032415.7(CARD11):c.3454G>A (p.Asp1152Asn)	rs147422861	0.00217
NM_032415.7(CARD11):c.1581C>A (p.His527Gln)	rs74876622	0.00182
NM_032415.7(CARD11):c.3025G>A (p.Val1009Ile)	rs147381531	0.00138
NM_032415.7(CARD11):c.1262T>C (p.Met421Thr)	rs372864426	0.00113
NM_032415.7(CARD11):c.3059C>T (p.Thr1020Met)	rs116583746	0.00102
NM_032415.7(CARD11):c.2060C>T (p.Ala687Val)	rs41493047	0.00088
NM_032415.7(CARD11):c.1975G>A (p.Val659Met)	rs78443994	0.00063
NM_032415.7(CARD11):c.2641A>G (p.Ser881Gly)	rs140097633	0.00063
NM_032415.7(CARD11):c.1741G>A (p.Ala581Thr)	rs75403455	0.00056
NM_032415.7(CARD11):c.572A>G (p.Asn191Ser)	rs147264763	0.00051
NM_032415.7(CARD11):c.2119C>T (p.Arg707Cys)	rs143049136	0.00039
NM_032415.7(CARD11):c.1595C>T (p.Thr532Met)	rs201780608	0.00021
NM_032415.7(CARD11):c.3139G>A (p.Ala1047Thr)	rs146334064	0.00020
NM_032415.7(CARD11):c.2120G>A (p.Arg707His)	rs201948130	0.00002
NM_032415.7(CARD11):c.1823G>A (p.Arg608His)	rs587778150	0.00001
NM_032415.7(CARD11):c.2074G>A (p.Val692Met)	rs587778151	0.00001
NM_032415.7(CARD11):c.2242A>G (p.Thr748Ala)	rs376122142
NM_032415.7(CARD11):c.2298G>T (p.Glu766Asp)	rs534947493
NM_032415.7(CARD11):c.2395G>A (p.Asp799Asn)	rs587778152
NM_032415.7(CARD11):c.590T>C (p.Val197Ala)	rs587778153

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