"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SNX19"[gen - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2642548	NM_014758.3(SNX19):c.2973C>G (p.Ser991=)	SNX19	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 720700	NM_014758.3(SNX19):c.949A>G (p.Ser317Gly)	SNX19 (S317G)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 1694653	GRCh37/hg19 11q24.3-25(chr11:128634685-134257741)x1	ACAD8, ADAMTS15 +28 more	Copy number loss	not provided	GPathogenic

Format

Sort by

Choose Destination