"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "NDN"[ge - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 445448	NM_002487.3(NDN):c.953T>C (p.Val318Ala)	NDN (V318A)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 735177	NM_002487.3(NDN):c.949A>G (p.Ser317Gly)	NDN (S317G)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2796505	NM_002487.3(NDN):c.858C>T (p.Asp286=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 735178	NM_002487.3(NDN):c.768C>T (p.Pro256=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791096	NM_002487.3(NDN):c.690C>T (p.Asp230=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 762141	NM_002487.3(NDN):c.649C>T (p.Leu217=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 713375	NM_002487.3(NDN):c.263C>T (p.Pro88Leu)	NDN (P88L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 743270	NM_002487.3(NDN):c.174C>G (p.Pro58=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 754947	NM_002487.3(NDN):c.117A>G (p.Ala39=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 779158	NM_002487.3(NDN):c.51C>A (p.Ala17=)	NDN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3243892	NC_000015.9:g.(?_23889140)_(23932364_?)del	MAGEL2, NDN	Deletion	not provided	GUncertain significance
Select item 2426508	NC_000015.9:g.(?_23006221)_(23932364_?)del	GOLGA6L2, MAGEL2 +4 more	Deletion	not provided	GUncertain significance
Select item 1447182	NC_000015.9:g.(?_23006221)_(23932364_?)dup	GOLGA6L2, MAGEL2 +4 more	Duplication	not provided	GUncertain significance