List of variants in gene TNFRSF13B reported as benign for B cell deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.81G>A (p.Thr27=)	rs8072293	0.81820
NM_012452.3(TNFRSF13B):c.831T>C (p.Ser277=)	rs11078355	0.48964
NM_012452.3(TNFRSF13B):c.445+25A>C	rs2274892	0.35819
NM_012452.3(TNFRSF13B):c.752C>T (p.Pro251Leu)	rs34562254	0.12363
NM_012452.3(TNFRSF13B):c.291T>G (p.Pro97=)	rs35062843	0.03423
NM_012452.3(TNFRSF13B):c.563A>T (p.Lys188Met)	rs74811083	0.01589
NM_012452.3(TNFRSF13B):c.659T>C (p.Val220Ala)	rs56063729	0.01586
NM_012452.3(TNFRSF13B):c.61+10C>T	rs148297590	0.00621
NM_012452.3(TNFRSF13B):c.618C>T (p.Ala206=)	rs147846226	0.00133
NM_012452.3(TNFRSF13B):c.415T>C (p.Leu139=)	rs141494621	0.00121
NM_012452.3(TNFRSF13B):c.605G>A (p.Arg202His)	rs104894649	0.00076
NM_012452.3(TNFRSF13B):c.570G>A (p.Gly190=)	rs199810075	0.00026
NM_012452.3(TNFRSF13B):c.126T>C (p.Pro42=)	rs377551435	0.00011
NM_012452.3(TNFRSF13B):c.86_88del	rs150068036
NM_012452.3(TNFRSF13B):c.199+12G>A
NM_012452.3(TNFRSF13B):c.560AGA[1] (p.Lys188del)	rs376630110

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