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 | LOC105375355 SRRM3 LOC100133091 ZP3 DTX2P1-UPK3BP1-PMS2P11 POMZP3 HSPB1 SSC4D SPDYE16 YWHAG FDPSP2 DTX2 |
nsv428174 | Chr.7:76305019 - 77220062 on Build GRCh38 | Gain | ZP3 DTX2P1-UPK3BP1-PMS2P11 POMZP3 SPDYE17 PMS2P9 SSC4D SPDYE16 YWHAG FDPSP2 LOC105375355 SPDYE18 LOC100133091 FGL2 CCDC146 DTX2 |
nsv528969 | Chr.7:75074053 - 76920728 on Build GRCh38 | Gain | STAG3L1 ZP3 PMS2P10 SSC4D SPDYE16 YWHAG STYXL1 SPDYE5 CCL26 LOC107986711 LOC100133091 LOC541473 PMS2P3 HSPB1 RHBDD2 LOC441259 GTF2IP1 TMEM120A POM121C TRIM73 HIP1 PMS2P2 POMZP3 GTF2IRD2B MIR4651 FDPSP2 LOC105375355 SRRM3 SNORA14A GTF2IP7 POR NSUN5P1 NCF1C CCL24 MDH2 DTX2 |
nsv1028665 | Chr.7:76336044 - 76445651 on Build GRCh38 | Gain | ZP3 SSC4D YWHAG |
dgv120n16 | Chr.7:75440769 - 76641919 on Build GRCh38 | Deletion | ZP3 SSC4D SPDYE16 YWHAG STYXL1 SPDYE5 CCL26 LOC107986711 LOC100133091 PMS2P3 HSPB1 RHBDD2 TMEM120A POM121C HIP1 POMZP3 MIR4651 FDPSP2 LOC105375355 SRRM3 SNORA14A GTF2IP7 POR CCL24 MDH2 DTX2 |
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 |