ClinVar Miner

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

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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NM_032415.6(CARD11):c.1212G>A (p.Arg404=) rs142108678
NM_032415.6(CARD11):c.1260G>A (p.Glu420=) rs112171353
NM_032415.6(CARD11):c.1440G>A (p.Ser480=) rs41396348
NM_032415.6(CARD11):c.1590A>C (p.Glu530Asp) rs41515445
NM_032415.6(CARD11):c.1695C>T (p.Ala565=) rs41454944
NM_032415.6(CARD11):c.180G>T (p.Val60=) rs117016854
NM_032415.6(CARD11):c.225G>C (p.Arg75=) rs10229368
NM_032415.6(CARD11):c.2670G>A (p.Ser890=) rs146545469
NM_032415.6(CARD11):c.2748C>T (p.Asn916=) rs61731201
NM_032415.6(CARD11):c.2913C>T (p.Cys971=) rs61757651
NM_032415.6(CARD11):c.3019+6C>T rs199705831
NM_032415.6(CARD11):c.3019+7G>A rs184926618
NM_032415.6(CARD11):c.3019+9C>T rs200741645
NM_032415.6(CARD11):c.3090C>T (p.Asn1030=) rs112241277
NM_032415.6(CARD11):c.3144+9G>A rs112606562
NM_032415.6(CARD11):c.3399C>T (p.Arg1133=) rs117428786

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