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

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2687955	NM_000625.4(NOS2):c.2757A>G (p.Thr919=)	NOS2	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2687956	NM_000625.4(NOS2):c.2428+6C>T	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687957	NM_000625.4(NOS2):c.2358T>C (p.Gly786=)	NOS2	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688094	NM_000625.4(NOS2):c.1859+88G>T	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688228	NM_000625.4(NOS2):c.1823C>T (p.Ser608Leu)	NOS2 (S608L)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2687962	NM_000625.4(NOS2):c.1477-52T>C	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688348	NM_000625.4(NOS2):c.1476+51TG[10]	NOS2	Microsatellite (intron variant)	not specified	GBenign
Select item 2688145	NM_000625.4(NOS2):c.1476+46C>T	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688251	NM_000625.4(NOS2):c.1155C>T (p.Asp385=)	NOS2	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2687960	NM_000625.4(NOS2):c.864+22A>G	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687961	NM_000625.4(NOS2):c.722+11A>G	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688120	NM_000625.4(NOS2):c.-73-10C>T	NOS2	Single nucleotide variant (intron variant)	not specified	GBenign