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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2687943	NM_021035.3(ZNFX1):c.4189C>T (p.Leu1397=)	ZNFX1	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2687966	NM_021035.3(ZNFX1):c.4052C>T (p.Thr1351Ile)	ZNFX1 (T1351I)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2688233	NM_021035.3(ZNFX1):c.3777G>A (p.Met1259Ile)	ZNFX1 (M1259I)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2688234	NM_021035.3(ZNFX1):c.2805-11C>G	ZNFX1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687967	NM_021035.3(ZNFX1):c.2804+18T>C	ZNFX1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687973	NM_021035.3(ZNFX1):c.2772G>C (p.Gln924His)	ZNFX1 (Q924H)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2688235	NM_021035.3(ZNFX1):c.2613T>C (p.His871=)	ZNFX1	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2688026	NM_021035.3(ZNFX1):c.1871-90A>T	ZNFX1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687945	NM_021035.3(ZNFX1):c.1665C>T (p.Tyr555=)	ZNFX1	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2687968	NM_021035.3(ZNFX1):c.61+46A>G	ZNFX1	Single nucleotide variant (intron variant)	not specified	GBenign