"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "FREM3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2655103	NM_001168235.2(FREM3):c.5994C>T (p.Thr1998=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2655104	NM_001168235.2(FREM3):c.2847T>C (p.Ser949=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2655105	NM_001168235.2(FREM3):c.2067C>T (p.His689=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2655106	NM_001168235.2(FREM3):c.1695T>C (p.Phe565=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2655107	NM_001168235.2(FREM3):c.1431A>G (p.Arg477=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2655108	NM_001168235.2(FREM3):c.933C>T (p.Ala311=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	TMA16, CXCL1 +537 more	Copy number gain	not provided	GPathogenic
Select item 624488	GRCh37/hg19 4q31.21(chr4:144612898-144744643)x3	FREM3	Copy number gain	not provided	GLikely benign

ClinVar