Assay Details
Target Gene Details
Entrez Gene ID: | 7991 |
Gene Name: | tumor suppressor candidate 3 |
Gene Aliases: |
D8S1992, M33, MRT22, MRT7, N33, OST3A |
Location: |
Chr.8:15540087-15766649 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TUSC3 | NM_006765.3 | NP_006756.2 | ||
NM_178234.2 | NP_839952.1 | |||
BC010370.1 | AAH10370.1 | |||
BT020002.1 | AAV38805.1 | |||
DA796279.1 | ||||
U42349.1 | AAB18374.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv437055 | Chr.8:15398926 - 15806828 on Build GRCh38 | Loss | TUSC3 |
nsv6089 | Chr.8:15538984 - 15565828 on Build GRCh38 | Deletion | TUSC3 |
esv2759598 | Chr.8:14768691 - 15907197 on Build GRCh38 | Loss | MIR383 SGCZ TUSC3 |
dgv248e55 | Chr.8:14773418 - 15806518 on Build GRCh38 | Loss | MIR383 SGCZ TUSC3 |
nsv465564 | Chr.8:15562617 - 15585104 on Build GRCh38 | Loss | TUSC3 |
nsv610556 | Chr.8:15562268 - 15585104 on Build GRCh38 | Gain | TUSC3 |
dgv873n27 | Chr.8:15545427 - 15569939 on Build GRCh38 | Loss | TUSC3 |
esv3584880 | Chr.8:15555938 - 15576174 on Build GRCh38 | Loss | TUSC3 |
nsv1034460 | Chr.8:15555926 - 15683272 on Build GRCh38 | Loss | TUSC3 |
nsv1029399 | Chr.8:14978756 - 16296799 on Build GRCh38 | Gain | SGCZ TUSC3 MSR1 |
nsv8298 | Chr.8:14772387 - 15806223 on Build GRCh38 | Gain+Loss | MIR383 SGCZ TUSC3 |
dgv265n111 | Chr.8:15553858 - 15583077 on Build GRCh38 | Deletion | TUSC3 |
nsv610554 | Chr.8:15554099 - 15589367 on Build GRCh38 | Loss | TUSC3 |
esv3616403 | Chr.8:15528780 - 15600263 on Build GRCh38 | Loss | TUSC3 |
esv3584881 | Chr.8:15543669 - 15576174 on Build GRCh38 | Loss | TUSC3 |
esv3616407 | Chr.8:15544186 - 15580033 on Build GRCh38 | Loss | TUSC3 |
nsv514477 | Chr.8:15545759 - 15569957 on Build GRCh38 | Loss | TUSC3 |
nsv951108 | Chr.8:15559192 - 15579191 on Build GRCh38 | Deletion | TUSC3 |
dgv7107n100 | Chr.8:15545539 - 15576162 on Build GRCh38 | Loss | TUSC3 |
nsv610466 | Chr.8:14469128 - 15809390 on Build GRCh38 | Loss | MIR383 SGCZ TUSC3 |
nsv818605 | Chr.8:14773392 - 15802730 on Build GRCh38 | Loss | MIR383 SGCZ TUSC3 |
nsv610524 | Chr.8:15419198 - 15568674 on Build GRCh38 | Loss | TUSC3 |
nsv1161735 | Chr.8:15543415 - 15565761 on Build GRCh38 | Deletion | TUSC3 |
dgv2049e212 | Chr.8:15543403 - 15565761 on Build GRCh38 | Loss | TUSC3 |
nsv6090 | Chr.8:15553229 - 15586844 on Build GRCh38 | Insertion | TUSC3 |
nsv1020054 | Chr.8:15444894 - 15812092 on Build GRCh38 | Gain | TUSC3 |
More Information
Additional Information:
For this assay, SNP(s) [rs78221014] 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 |