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: 30
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HGVS dbSNP
NM_032415.6(CARD11):c.1008G>A (p.Leu336=) rs1554275179
NM_032415.6(CARD11):c.1017+3G>A rs371474461
NM_032415.6(CARD11):c.1101G>A (p.Thr367=) rs368714967
NM_032415.6(CARD11):c.1262T>C (p.Met421Thr) rs372864426
NM_032415.6(CARD11):c.1425C>T (p.Asp475=) rs370885250
NM_032415.6(CARD11):c.1519-7C>T rs370431421
NM_032415.6(CARD11):c.1581C>A (p.His527Gln) rs74876622
NM_032415.6(CARD11):c.1595C>T (p.Thr532Met) rs201780608
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.16C>A (p.Pro6Thr) rs191347765
NM_032415.6(CARD11):c.1710C>T (p.Asn570=) rs753114537
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.2081C>T (p.Ser694Leu) rs3735133
NM_032415.6(CARD11):c.2244G>A (p.Thr748=) rs3735131
NM_032415.6(CARD11):c.2270-4G>A rs371703131
NM_032415.6(CARD11):c.2436C>T (p.His812=) rs146943681
NM_032415.6(CARD11):c.2479C>T (p.Leu827=) rs767482937
NM_032415.6(CARD11):c.2718C>T (p.Ser906=) rs916415454
NM_032415.6(CARD11):c.2856C>T (p.Ser952=) rs115741110
NM_032415.6(CARD11):c.2946C>T (p.Thr982=) rs200612985
NM_032415.6(CARD11):c.2961G>A (p.Thr987=) rs368214396
NM_032415.6(CARD11):c.3019+8G>A rs754091988
NM_032415.6(CARD11):c.3025G>A (p.Val1009Ile) rs147381531
NM_032415.6(CARD11):c.3059C>T (p.Thr1020Met) rs116583746
NM_032415.6(CARD11):c.3060G>A (p.Thr1020=) rs138682139
NM_032415.6(CARD11):c.3454G>A (p.Asp1152Asn) rs147422861
NM_032415.6(CARD11):c.705G>A (p.Arg235=) rs111292123
NM_032415.6(CARD11):c.945C>T (p.Asp315=) rs149430714

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