CXCL16[gene] and "single gene"[properties] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2400669	NM_001386809.1(CXCL16):c.662C>T (p.Ala221Val)	CXCL16 (A221V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3079175	NM_001386809.1(CXCL16):c.619C>A (p.Pro207Thr)	CXCL16 (P207T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476001	NM_001386809.1(CXCL16):c.610G>A (p.Ala204Thr)	CXCL16 (A204T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777096	NM_001386809.1(CXCL16):c.575C>T (p.Pro192Leu)	CXCL16 (P192L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2320073	NM_001386809.1(CXCL16):c.428C>G (p.Ser143Cys)	CXCL16 (S143C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207631	NM_001386809.1(CXCL16):c.421C>T (p.Leu141Phe)	CXCL16 (L141F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555485	NM_001386809.1(CXCL16):c.388G>A (p.Ala130Thr)	CXCL16 (A130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079174	NM_001386809.1(CXCL16):c.320C>T (p.Ser107Leu)	CXCL16 (S107L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3270403	NM_001386809.1(CXCL16):c.292G>C (p.Asp98His)	CXCL16 (D98H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079173	NM_001386809.1(CXCL16):c.262C>G (p.Pro88Ala)	CXCL16 (P88A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079172	NM_001386809.1(CXCL16):c.98G>A (p.Ser33Asn)	CXCL16 (S33N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541905	NM_001386809.1(CXCL16):c.17G>T (p.Arg6Leu)	CXCL16 (R6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210695	NM_001386809.1(CXCL16):c.5G>A (p.Gly2Glu)	CXCL16 (G2E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272043	NM_001386809.1(CXCL16):c.-29C>T	CXCL16	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 777097	NM_001386809.1(CXCL16):c.-49G>A	CXCL16	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign