"Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan"[submitte - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688069	NM_003177.7(SYK):c.-41-37G>A	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688110	NM_003177.7(SYK):c.417+79A>G	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688027	NM_003177.7(SYK):c.846+105C>T	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688084	NM_003177.7(SYK):c.847-66G>A	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688172	NM_003177.7(SYK):c.1003+91G>A	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688051	NM_003177.7(SYK):c.1065C>T (p.Pro355=)	SYK	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688259	NM_003177.7(SYK):c.1182-7C>G	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688052	NM_003177.7(SYK):c.1302G>C (p.Arg434=)	SYK	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688054	NM_003177.7(SYK):c.1338G>A (p.Leu446=)	SYK	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688070	NM_003177.7(SYK):c.1391+58C>T	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688090	NM_003177.7(SYK):c.1391+69C>T	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688055	NM_003177.7(SYK):c.1521C>T (p.Tyr507=)	SYK	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688111	NM_003177.7(SYK):c.1545T>C (p.Leu515=)	SYK	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688074	NM_003177.7(SYK):c.1581+47G>A	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688260	NM_003177.7(SYK):c.1582-16T>A	SYK	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687942	NM_003177.7(SYK):c.1836-49A>T	SYK	Single nucleotide variant (intron variant)	not specified	GBenign