ClinVar Miner

List of variants in gene CARD11 reported as likely benign for BENTA disease

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_032415.6(CARD11):c.1008G>A (p.Leu336=) rs1554275179
NM_032415.6(CARD11):c.1101G>A (p.Thr367=) rs368714967
NM_032415.6(CARD11):c.1581C>A (p.His527Gln) rs74876622
NM_032415.6(CARD11):c.1610G>C (p.Ser537Thr) rs148753096
NM_032415.6(CARD11):c.1630A>C (p.Ile544Leu) rs147687933
NM_032415.6(CARD11):c.1692C>T (p.Thr564=) rs752788421
NM_032415.6(CARD11):c.1887T>C (p.Asp629=) rs150116627
NM_032415.6(CARD11):c.2060C>T (p.Ala687Val) rs41493047
NM_032415.6(CARD11):c.2270-4G>A rs371703131
NM_032415.6(CARD11):c.2479C>T (p.Leu827=) rs767482937
NM_032415.6(CARD11):c.3025G>A (p.Val1009Ile) rs147381531
NM_032415.6(CARD11):c.3454G>A (p.Asp1152Asn) rs147422861

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