Hs02650683_cn

• Gene Symbol: SLFN12
• Assay Reference Genome Location: Chr.17:35422697 on build GRCh38
• Cytoband: 17q12

Target Gene Details

• Entrez Gene ID: 55106
• Gene Name: schlafen family member 12
• Gene Aliases: SLFN3
• Location: Chr.17:35406684-35433176 on Build GRCh38
• Assay Gene Location: Within Exon 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLFN12	NM_001289009.1	2	644	NP_001275938.1
	NM_018042.4	2	709	NP_060512.3
	XM_005257995.4	3	600	XP_005258052.1
	XM_011524967.2	4	722	XP_011523269.1
	XM_017024809.1	2	533	XP_016880298.1
	XM_017024810.1	3	1190	XP_016880299.1
	XM_017024811.1	4	722	XP_016880300.1
	AK001122.1	2	685	BAA91512.1
	AK291826.1	2	622
	BC035605.1	2	709	AAH35605.1
	BX647081.1	5	832

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv457728	Chr.17:35357016 - 35441180 on Build GRCh38	Gain	SLFN12 LOC105371933 SLFN11 SLFN13
esv2762399	Chr.17:35349487 - 35441180 on Build GRCh38	Loss	SLFN12 LOC105371933 SLFN11 SLFN13
dgv907e212	Chr.17:35349475 - 35442775 on Build GRCh38	Loss	SLFN12 LOC105371933 SLFN11 SLFN13
dgv5533n54	Chr.17:35404745 - 35433147 on Build GRCh38	Loss	SLFN12
nsv1060927	Chr.17:35357088 - 35423226 on Build GRCh38	Gain	SLFN12 LOC105371933 SLFN11
nsv574743	Chr.17:35337025 - 35447140 on Build GRCh38	Loss	SLFN12 LOC105371933 SLFN11 SLFN13
dgv3142n100	Chr.17:35344137 - 35442187 on Build GRCh38	Loss	SLFN12 LOC105371933 SLFN11 SLFN13
nsv515566	Chr.17:35337799 - 35441180 on Build GRCh38	Gain+Loss	SLFN12 LOC105371933 SLFN11 SLFN13
esv3892999	Chr.17:35252863 - 35925533 on Build GRCh38	Loss	LOC105371743 SLFN12 RDM1 RASL10B SLFN14 C17orf50 AP2B1 SLFN12L MMP28 HEATR9 CCL5 LOC105371933 PEX12 SNORD7 SLFN11 LRRC37A8P SLFN5 GAS2L2 SLFN13 TAF15
dgv571e214	Chr.17:35353236 - 35442365 on Build GRCh38	Gain	SLFN12 LOC105371933 SLFN11 SLFN13
esv2715869	Chr.17:35351977 - 35440321 on Build GRCh38	Deletion	SLFN12 LOC105371933 SLFN11 SLFN13
nsv574741	Chr.17:35225256 - 35500115 on Build GRCh38	Loss	LOC105371932 SLFN12 LOC105371933 SLFN11 SLFN5 SLFN13 SLFN12L

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Function(s)

ATP binding