"Ambry Genetics"[submitter] AND "TNFSF12-TNFSF13"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2535301	NM_003809.3(TNFSF12):c.647T>C (p.Leu216Ser)	TNFSF12, TNFSF12-TNFSF13 (L216S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 837160	NM_003809.3(TNFSF12):c.655C>T (p.Arg219Trp)	TNFSF12, TNFSF12-TNFSF13 (R219W)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 1427587	NM_003809.3(TNFSF12):c.662G>C (p.Gly221Ala)	TNFSF12, TNFSF12-TNFSF13 (G221A)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 649356	NM_003809.3(TNFSF12):c.673C>T (p.Arg225Trp)	TNFSF12, TNFSF12-TNFSF13 (R225W)	Single nucleotide variant (missense variant +2 more)	Common variable immunodeficiency +1 more	GUncertain significance
Select item 2383367	NM_003808.4(TNFSF13):c.25C>G (p.Leu9Val)	TNFSF12-TNFSF13, TNFSF13 (L9V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2282202	NM_003808.4(TNFSF13):c.38G>A (p.Gly13Glu)	TNFSF12-TNFSF13, TNFSF13 (G13E)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2595292	NM_003808.4(TNFSF13):c.113C>T (p.Ala38Val)	TNFSF12-TNFSF13, TNFSF13 (A21V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2534737	NM_003808.4(TNFSF13):c.190C>T (p.Arg64Trp)	TNFSF12-TNFSF13, TNFSF13 (R47W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2254220	NM_003808.4(TNFSF13):c.191G>A (p.Arg64Gln)	TNFSF12-TNFSF13, TNFSF13 (R64Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2264204	NM_003808.4(TNFSF13):c.330A>C (p.Lys110Asn)	TNFSF12-TNFSF13, TNFSF13 (K110N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242977	NM_003808.4(TNFSF13):c.394G>T (p.Asp132Tyr)	TNFSF12-TNFSF13, TNFSF13 (D212Y +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance