"GeneDx"[submitter] AND "NTNG1"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146007	GRCh38/hg38 1p21.3-13.3(chr1:97272349-108893138)x1	AGL, AKNAD1 +195 more	Copy number loss	See cases	GPathogenic
Select item 60005	GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1	AGL, AHCYL1 +333 more	Copy number loss	See cases	GPathogenic
Select item 60007	GRCh38/hg38 1p21.2-13.2(chr1:101618097-111703028)x1	ELAPOR1, EPS8L3 +276 more	Copy number loss	See cases	GPathogenic
Select item 57788	GRCh38/hg38 1p13.3(chr1:107042518-107326708)x3	LOC126805818, LOC129931063 +7 more	Copy number gain	See cases	GUncertain significance
Select item 1225285	NM_001113226.3(NTNG1):c.-293A>G	NTNG1	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1257521	NM_001113226.3(NTNG1):c.-120G>C	NTNG1	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1291153	NM_001113226.3(NTNG1):c.246+180T>C	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 783292	NM_001113226.3(NTNG1):c.846A>G (p.Ala282=)	NTNG1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1274913	NM_001113226.3(NTNG1):c.887+97C>T	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234257	NM_001113226.3(NTNG1):c.887+173A>C	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225825	NM_001113226.3(NTNG1):c.888-308C>G	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250495	NM_001113226.3(NTNG1):c.1087+10829A>G	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241235	NM_001113226.3(NTNG1):c.1087+10866G>A	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174969	NM_001113226.3(NTNG1):c.1365A>C (p.Gly455=)	NTNG1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1242404	NM_001113226.3(NTNG1):c.1390+258T>G	NTNG1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277489	NM_001113226.3(NTNG1):c.*127A>C	NTNG1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign