"PreventionGenetics, part of Exact Sciences"[submitter] AND "NTNG1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 738290	NM_001113226.3(NTNG1):c.381C>G (p.Pro127=)	NTNG1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 736031	NM_001113226.3(NTNG1):c.408G>A (p.Leu136=)	NTNG1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 715245	NM_001113226.3(NTNG1):c.430C>T (p.Leu144=)	NTNG1	Single nucleotide variant (synonymous variant)	NTNG1-related disorder +1 more	GBenign
Select item 3048525	NM_001113226.3(NTNG1):c.861G>A (p.Ala287=)	NTNG1	Single nucleotide variant (synonymous variant)	NTNG1-related disorder	GLikely benign
Select item 3024814	NM_001113226.3(NTNG1):c.1224T>C (p.Ser408=)	NTNG1	Single nucleotide variant (intron variant +1 more)	NTNG1-related disorder +1 more	GLikely benign
Select item 3052477	NM_001113226.3(NTNG1):c.1404C>T (p.Asp468=)	NTNG1	Single nucleotide variant (synonymous variant)	NTNG1-related disorder	GLikely benign

ClinVar