Assay Details
Target Gene Details
Entrez Gene ID: | 84070 |
Gene Name: | family with sequence similarity 186 member B |
Gene Aliases: |
C12orf25 |
Location: |
Chr.12:49582875-49605710 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM186B | NM_032130.2 | NP_115506.1 | ||
NR_027450.1 | ||||
XM_006719625.2 | XP_006719688.1 | |||
XM_006719626.2 | XP_006719689.1 | |||
XM_006719627.3 | XP_006719690.1 | |||
XM_011538796.2 | XP_011537098.1 | |||
XM_011538797.2 | XP_011537099.1 | |||
XM_017020008.1 | XP_016875497.1 | |||
AK093242.1 | ||||
AK302702.1 | ||||
AL136748.1 | CAB66682.1 | |||
BC035621.1 | AAH35621.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832406 | Chr.12:49466910 - 49668353 on Build GRCh38 | Loss | SPATS2 LOC100422296 FAM186B KCNH3 FMNL3 PRPF40B MCRS1 |
More Information
Additional Information:
For this assay, SNP(s) [rs79035034] 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 |