Assay Details
Target Gene Details
Entrez Gene ID: | 63939 |
Gene Name: | family with sequence similarity 217 member B |
Gene Aliases: |
C20orf177, dJ551D2.5 |
Location: |
Chr.20:59933764-59948680 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 3 - Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM217B | NM_001190826.1 | NP_001177755.1 | ||
NM_001190827.1 | NP_001177756.1 | |||
NM_022106.2 | NP_071389.1 | |||
XM_011528985.2 | XP_011527287.1 | |||
XM_011528986.2 | XP_011527288.1 | |||
AK125073.1 | ||||
AK304220.1 | ||||
BC020771.1 | ||||
BC054002.1 | AAH54002.1 | |||
DB476861.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1062669 | Chr.20:59878803 - 59940597 on Build GRCh38 | Loss | FAM217B PPP1R3D SYCP2 |
dgv4336n100 | Chr.20:59857564 - 59943263 on Build GRCh38 | Loss | FAM217B PPP1R3D SYCP2 |
nsv1065994 | Chr.20:59845169 - 59951828 on Build GRCh38 | Loss | FAM217B PPP1R3D SYCP2 PHACTR3 |
More Information
Additional Information:
For this assay, SNP(s) [rs74759139] 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 Non-exonic DGV Variation |