ClinVar Miner

List of variants in gene ZNF341 studied for B cell deficiency

Included ClinVar conditions (64):
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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001282933.2(ZNF341):c.2505T>C (p.Ala835=) rs2626551 0.74572
NM_001282933.2(ZNF341):c.340-20C>G rs142373708 0.00712
NM_001282933.2(ZNF341):c.366G>A (p.Pro122=) rs75946243 0.00643
NM_001282933.2(ZNF341):c.553C>T (p.Pro185Ser) rs45577437 0.00260
NM_001282933.2(ZNF341):c.2117C>T (p.Thr706Met) rs138992523 0.00215
NM_001282933.2(ZNF341):c.2542G>A (p.Val848Ile) rs143727353 0.00110
NM_001282933.2(ZNF341):c.2560G>A (p.Glu854Lys) rs145996048 0.00044
NM_001282933.2(ZNF341):c.910G>A (p.Ala304Thr) rs201763709 0.00034
NM_001282933.2(ZNF341):c.119C>T (p.Ala40Val) rs151120596 0.00008
NM_001282933.2(ZNF341):c.481C>T (p.Pro161Ser) rs775264826 0.00001
NM_001282933.2(ZNF341):c.904C>T (p.Arg302Ter) rs746141726 0.00001
NM_001282933.2(ZNF341):c.1054T>C (p.Cys352Arg) rs2122686345
NM_001282933.2(ZNF341):c.1083del (p.Lys362fs) rs1568945329
NM_001282933.2(ZNF341):c.1156C>T (p.Arg386Ter) rs982121798
NM_001282933.2(ZNF341):c.1647C>G (p.Tyr549Ter) rs376598954
NM_001282933.2(ZNF341):c.583C>T (p.Gln195Ter) rs1568940507
NM_001282933.2(ZNF341):c.98C>T (p.Pro33Leu)

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