Assay Details
Target Gene Details
Entrez Gene ID: | 7532 |
Gene Name: | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma |
Gene Aliases: |
14-3-3GAMMA, PPP1R170 |
Location: |
Chr.7:76326791-76359025 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
YWHAG | NM_012479.3 | NP_036611.2 | ||
AB024334.1 | BAA85184.1 | |||
AF142498.1 | AAD48408.1 | |||
AK024230.1 | ||||
AK293505.1 | ||||
AK295029.1 | ||||
BC020963.2 | AAH20963.1 | |||
CR541904.1 | CAG46702.1 | |||
CR541925.1 | CAG46723.1 | |||
DC343104.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2422494 | Chr.7:76286900 - 76984449 on Build GRCh38 | Duplication | LOC100133091 YWHAG FDPSP2 DTX2 POMZP3 DTX2P1-UPK3BP1-PMS2P11 ZP3 LOC105375355 SSC4D HSPB1 SRRM3 SPDYE16 |
nsv428174 | Chr.7:76305019 - 77220062 on Build GRCh38 | Gain | LOC100133091 PMS2P9 YWHAG FDPSP2 DTX2 POMZP3 DTX2P1-UPK3BP1-PMS2P11 LOC105375355 FGL2 SPDYE18 SSC4D CCDC146 SPDYE17 ZP3 SPDYE16 |
nsv528969 | Chr.7:75074053 - 76920728 on Build GRCh38 | Gain | YWHAG POMZP3 LOC105375355 NSUN5P1 SSC4D SRRM3 LOC541473 PMS2P2 STYXL1 MIR4651 SNORA14A ZP3 TRIM73 PMS2P10 GTF2IRD2B RHBDD2 HSPB1 POM121C MDH2 SPDYE16 LOC100133091 POR TMEM120A FDPSP2 DTX2 STAG3L1 CCL26 HIP1 NCF1C LOC107986711 LOC441259 CCL24 GTF2IP7 SPDYE5 GTF2IP1 PMS2P3 |
nsv1028665 | Chr.7:76336044 - 76445651 on Build GRCh38 | Gain | YWHAG ZP3 SSC4D |
dgv120n16 | Chr.7:75440769 - 76641919 on Build GRCh38 | Deletion | YWHAG POMZP3 LOC105375355 SSC4D SRRM3 STYXL1 MIR4651 SNORA14A ZP3 RHBDD2 HSPB1 POM121C MDH2 SPDYE16 LOC100133091 POR TMEM120A FDPSP2 DTX2 CCL26 HIP1 LOC107986711 CCL24 GTF2IP7 SPDYE5 PMS2P3 |
More Information
Additional Information:
For this assay, SNP(s) [rs73359657] 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 |