"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "NCDN"[gene - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1701099	NM_014284.3(NCDN):c.175-4A>G	NCDN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1879083	NM_014284.3(NCDN):c.225G>T (p.Arg75=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1694506	NM_014284.3(NCDN):c.240C>T (p.Val80=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638646	NM_014284.3(NCDN):c.270C>A (p.Thr90=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3067426	NM_014284.3(NCDN):c.363C>T (p.Ala121=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638647	NM_014284.3(NCDN):c.661G>A (p.Val221Met)	NCDN (V204M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2638648	NM_014284.3(NCDN):c.860G>A (p.Arg287His)	NCDN (R270H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2210583	NM_014284.3(NCDN):c.974C>T (p.Thr325Met)	NCDN (T308M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3025892	NM_014284.3(NCDN):c.1098C>T (p.Ser366=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2405199	NM_014284.3(NCDN):c.1349C>T (p.Thr450Ile)	NCDN (T433I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2638649	NM_014284.3(NCDN):c.1524G>A (p.Ser508=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638650	NM_014284.3(NCDN):c.1599G>A (p.Pro533=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638651	NM_014284.3(NCDN):c.1753+1G>A	NCDN	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 2638652	NM_014284.3(NCDN):c.1840G>A (p.Gly614Ser)	NCDN (G597S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2638653	NM_014284.3(NCDN):c.1872T>C (p.Pro624=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638654	NM_014284.3(NCDN):c.1968C>T (p.Pro656=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638655	NM_014284.3(NCDN):c.1992G>A (p.Pro664=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1694507	NM_014284.3(NCDN):c.2043C>T (p.Pro681=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1694508	NM_014284.3(NCDN):c.2138C>T (p.Thr713Met)	NCDN (T696M +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2582855	NM_014284.3(NCDN):c.2148C>T (p.His716=)	NCDN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar

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Items: 20