Hs04674256_cn

• Gene Symbol: FAM228A
• Assay Reference Genome Location: Chr.2:24182320 on build GRCh38
• Cytoband: 2p23.3

Target Gene Details

• Entrez Gene ID: 653140
• Gene Name: family with sequence similarity 228 member A
• Gene Aliases: C2orf84
• Location: Chr.2:24175043-24191698 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM228A	NM_001040710.2			NP_001035800.1
	BC050462.1			AAH50462.1
	HY022970.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv581179	Chr.2:24114991 - 24317722 on Build GRCh38	Gain	FAM228A FAM228B PFN4 ITSN2
nsv997445	Chr.2:23357900 - 24374347 on Build GRCh38	Gain	FAM228B SF3B6 PFN4 ITSN2 TP53I3 MFSD2B WDCP UBXN2A KLHL29 FAM228A FKBP1B LOC105374325 ATAD2B
nsv997725	Chr.2:24052436 - 25123406 on Build GRCh38	Gain	FAM228B SF3B6 DNAJC27 DNAJC27-AS1 PTRHD1 PFN4 ITSN2 EFR3B TP53I3 CENPO FAM228A FKBP1B ADCY3 NCOA1

More Information

Additional Information:

For this assay, SNP(s) [rs142051385] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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