"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "COL23A1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656126	NM_173465.4(COL23A1):c.1422C>T (p.Pro474=)	COL23A1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656127	NM_173465.4(COL23A1):c.1266G>A (p.Pro422=)	COL23A1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign

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