Assay Details
Target Gene Details
Entrez Gene ID: | 285315 |
Gene Name: | chromosome 3 open reading frame 33 |
Gene Aliases: |
AC3-33 |
Location: |
Chr.3:155762612-155806287 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C3orf33 | NM_001308229.1 | 5 | 726 | NP_001295158.1 |
NM_173657.2 | 6 | 853 | NP_775928.1 | |
XM_005247379.4 | 5 | 1698 | XP_005247436.1 | |
XM_011512710.2 | 4 | 651 | XP_011511012.1 | |
XM_011512711.2 | 5 | 830 | XP_011511013.1 | |
AF115515.1 | 5 | 689 | AAO06952.1 | |
AK055701.1 | 6 | 832 | BAB70989.1 | |
AK289890.1 | 5 | 726 | ||
AL832165.1 | 5 | 711 | ||
BC042198.1 | 5 | 688 | AAH42198.1 | |
BC064898.1 | 5 | 698 | AAH64898.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv592081 | Chr.3:155763308 - 155776126 on Build GRCh38 | Gain | C3orf33 |
esv25006 | Chr.3:155761458 - 155794985 on Build GRCh38 | Gain | C3orf33 |
nsv441844 | Chr.3:155763307 - 155774388 on Build GRCh38 | Gain | C3orf33 |
nsv592079 | Chr.3:155757090 - 155776126 on Build GRCh38 | Gain | C3orf33 |
esv3575619 | Chr.3:155751288 - 155774530 on Build GRCh38 | Gain | C3orf33 |
dgv4927n100 | Chr.3:155758758 - 155774388 on Build GRCh38 | Gain | C3orf33 |
esv3598284 | Chr.3:155760377 - 155780857 on Build GRCh38 | Loss | C3orf33 |
nsv1009618 | Chr.3:155652245 - 155774388 on Build GRCh38 | Gain | C3orf33 PLCH1 |
esv3598283 | Chr.3:155759067 - 155869415 on Build GRCh38 | Loss | C3orf33 SLC33A1 |
nsv514997 | Chr.3:155763277 - 155773949 on Build GRCh38 | Loss | C3orf33 |
esv3575620 | Chr.3:155757648 - 155796064 on Build GRCh38 | Gain | C3orf33 |
esv33346 | Chr.3:155763431 - 155780652 on Build GRCh38 | Gain | C3orf33 |
nsv592080 | Chr.3:155761433 - 155794055 on Build GRCh38 | Gain | C3orf33 |
dgv4926n100 | Chr.3:155757649 - 155797695 on Build GRCh38 | Gain | C3orf33 |
More Information
Additional Information:
For this assay, SNP(s) [rs113890115] 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 |