Hs04465444_cn

• Gene Symbol: SLFN12L
• Assay Reference Genome Location: Chr.17:35496421 on build GRCh38
• Cytoband: 17q12

Target Gene Details

• Entrez Gene ID: 100506736
• Gene Name: schlafen family member 12 like
• Gene Aliases: -
• Location: Chr.17:35474906-35537861 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLFN12L	XM_017024005.1			XP_016879494.1
	XM_017024006.1			XP_016879495.1
	XM_017024007.1			XP_016879496.1
	XM_017024008.1			XP_016879497.1
	XM_017024009.1			XP_016879498.1
	AK172761.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv2715870	Chr.17:35496129 - 35505261 on Build GRCh38	Deletion	SLFN12L
esv2676058	Chr.17:35493926 - 35498273 on Build GRCh38	Deletion	SLFN12L
esv3640451	Chr.17:35482860 - 35501389 on Build GRCh38	Loss	SLFN12L
esv3892999	Chr.17:35252863 - 35925533 on Build GRCh38	Loss	SNORD7 SLFN14 SLFN13 RASL10B RDM1 HEATR9 GAS2L2 SLFN5 MMP28 LOC105371743 SLFN11 PEX12 LOC105371933 SLFN12L CCL5 AP2B1 SLFN12 LRRC37A8P TAF15 C17orf50
nsv574741	Chr.17:35225256 - 35500115 on Build GRCh38	Loss	LOC105371933 SLFN12L LOC105371932 SLFN13 SLFN12 SLFN5 SLFN11

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Gene Ontology Categories:

Function(s)

ATP binding