"Illumina Laboratory Services, Illumina"[submitter] AND "TNFRSF13B"[ge - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322018	NM_012452.3(TNFRSF13B):c.*414G>A	TNFRSF13B	Single nucleotide variant (3 prime UTR variant)	Common Variable Immune Deficiency, Dominant	GBenign
Select item 322019	NM_012452.3(TNFRSF13B):c.*371C>T	TNFRSF13B	Single nucleotide variant (3 prime UTR variant)	Common Variable Immune Deficiency, Dominant	GUncertain significance
Select item 322020	NM_012452.3(TNFRSF13B):c.*353A>C	TNFRSF13B	Single nucleotide variant (3 prime UTR variant)	Common Variable Immune Deficiency, Dominant	GLikely benign
Select item 322021	NM_012452.3(TNFRSF13B):c.*226A>G	TNFRSF13B	Single nucleotide variant (3 prime UTR variant)	Common Variable Immune Deficiency, Dominant	GLikely benign
Select item 322022	NM_012452.3(TNFRSF13B):c.*173G>A	TNFRSF13B	Single nucleotide variant (3 prime UTR variant)	Common Variable Immune Deficiency, Dominant +1 more	GBenign
Select item 322023	NM_012452.3(TNFRSF13B):c.857C>A (p.Ala286Asp)	TNFRSF13B (A286D)	Single nucleotide variant (missense variant)	Common Variable Immune Deficiency, Dominant +1 more	GUncertain significance
Select item 260259	NM_012452.3(TNFRSF13B):c.831T>C (p.Ser277=)	TNFRSF13B	Single nucleotide variant (synonymous variant)	Common Variable Immune Deficiency, Dominant +3 more	GBenign
Select item 322024	NM_012452.3(TNFRSF13B):c.797C>T (p.Thr266Ile)	TNFRSF13B (T266I)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 322025	NM_012452.3(TNFRSF13B):c.752C>T (p.Pro251Leu)	TNFRSF13B (P251L)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 2 +3 more	GBenign
Select item 36878	NM_012452.3(TNFRSF13B):c.659T>C (p.Val220Ala)	TNFRSF13B (V220A)	Single nucleotide variant (missense variant)	Common Variable Immune Deficiency, Dominant +2 more	GBenign/Likely benign
Select item 5304	NM_012452.3(TNFRSF13B):c.605G>A (p.Arg202His)	TNFRSF13B (R202H)	Single nucleotide variant (missense variant)	Common Variable Immune Deficiency, Dominant +3 more	GConflicting classifications of pathogenicity
Select item 322026	NM_012452.3(TNFRSF13B):c.592C>T (p.Arg198Cys)	TNFRSF13B (R198C)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 235322	NM_012452.3(TNFRSF13B):c.563A>T (p.Lys188Met)	TNFRSF13B (K188M)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 5302	NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	TNFRSF13B (C104R)	Single nucleotide variant (missense variant)	TNFRSF13B-related condition +23 more	GConflicting classifications of pathogenicity; risk factor
Select item 260258	NM_012452.3(TNFRSF13B):c.291T>G (p.Pro97=)	TNFRSF13B	Single nucleotide variant (synonymous variant)	Immunodeficiency, common variable, 2 +2 more	GBenign/Likely benign
Select item 322027	NM_012452.3(TNFRSF13B):c.215G>A (p.Arg72His)	TNFRSF13B (R72H)	Single nucleotide variant (missense variant)	Immunoglobulin A deficiency 2 +4 more	GLikely benign
Select item 322029	NM_012452.3(TNFRSF13B):c.204dup (p.Leu69fs)	TNFRSF13B (L69fs)	Duplication (frameshift variant)	Immunodeficiency, common variable, 2 +5 more	GConflicting classifications of pathogenicity
Select item 322028	NM_012452.3(TNFRSF13B):c.201G>C (p.Arg67Ser)	TNFRSF13B (R67S)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 2 +1 more	GUncertain significance
Select item 322030	NM_012452.3(TNFRSF13B):c.126T>C (p.Pro42=)	TNFRSF13B	Single nucleotide variant (synonymous variant)	Common Variable Immune Deficiency, Dominant +2 more	GConflicting classifications of pathogenicity
Select item 36879	NM_012452.3(TNFRSF13B):c.81G>A (p.Thr27=)	TNFRSF13B	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 322032	NM_012452.3(TNFRSF13B):c.61+10C>G	TNFRSF13B	Single nucleotide variant (intron variant)	Common Variable Immune Deficiency, Dominant	GUncertain significance
Select item 322031	NM_012452.3(TNFRSF13B):c.61+10C>T	TNFRSF13B	Single nucleotide variant (intron variant)	Immunodeficiency, common variable, 2 +3 more	GBenign/Likely benign
Select item 2671583	Single allele	LGALS9C, MIR33B +30 more	Duplication	not provided	GPathogenic

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Items: 23