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

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2345194	NM_007157.4(ZXDB):c.222G>C (p.Leu74Phe)	ZXDB (L74F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2660723	NM_007157.4(ZXDB):c.232A>C (p.Thr78Pro)	ZXDB (T78P)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2660724	NM_007157.4(ZXDB):c.235G>C (p.Asp79His)	ZXDB (D79H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2660725	NM_007157.4(ZXDB):c.245GCG[4] (p.Gly86_Gly89del)	ZXDB	Microsatellite (inframe_deletion)	not provided	GLikely benign
Select item 2660726	NM_007157.4(ZXDB):c.267C>T (p.Gly89=)	ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660727	NM_007157.4(ZXDB):c.498G>A (p.Ala166=)	LOC130068356, ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660728	NM_007157.4(ZXDB):c.792C>T (p.Ser264=)	LOC130068357, ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660729	NM_007157.4(ZXDB):c.795C>T (p.Gly265=)	LOC130068357, ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660730	NM_007157.4(ZXDB):c.1284T>C (p.Phe428=)	ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660731	NM_007157.4(ZXDB):c.1299A>G (p.Lys433=)	ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660732	NM_007157.4(ZXDB):c.2220G>A (p.Ser740=)	ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	AWAT2, BCLAF3 +568 more	Copy number gain	not provided	GUncertain significance