Assay Details
Target Gene Details
Entrez Gene ID: | 283461 |
Gene Name: | chromosome 12 open reading frame 40 |
Gene Aliases: |
HEL-206, HEL-S-94 |
Location: |
Chr.12:39626167-39908300 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C12orf40 | NM_001031748.3 | 8 | 1204 | NP_001026918.2 |
NM_001319247.1 | 8 | 1204 | NP_001306176.1 | |
NR_135051.1 | 7 | 1065 | ||
XM_005268806.3 | 7 | 1014 | XP_005268863.1 | |
XM_011538231.2 | 7 | 1241 | XP_011536533.1 | |
AK097445.1 | 7 | 1014 | BAC05057.1 | |
BC038754.1 | 8 | 1201 | AAH38754.2 | |
BC048120.1 | 8 | 1188 | ||
EU668334.1 | 7 | 1014 | ||
GQ472216.1 | 7 | 1014 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3629269 | Chr.12:39667551 - 39701177 on Build GRCh38 | Loss | C12orf40 |
esv3629266 | Chr.12:39648921 - 39753228 on Build GRCh38 | Loss | C12orf40 ABCD2 |
More Information
Additional Information:
For this assay, SNP(s) [rs115122052] 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 Exonic DGV Variation |