Assay Details
Target Gene Details
Entrez Gene ID: | 9704 |
Gene Name: | DEAH-box helicase 34 |
Gene Aliases: |
DDX34, HRH1 |
Location: |
Chr.19:47349281-47382704 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DHX34 | NM_014681.5 | NP_055496.2 | ||
XM_005259443.3 | XP_005259500.1 | |||
XM_011527550.2 | XP_011525852.1 | |||
XM_011527551.2 | XP_011525853.1 | |||
XM_017027524.1 | XP_016883013.1 | |||
AK123046.1 | ||||
AK297692.1 | ||||
AK304710.1 | ||||
BE677798.1 | ||||
D50924.1 | BAA09483.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1062949 | Chr.19:47344392 - 47388294 on Build GRCh38 | Gain | DHX34 |
esv2758765 | Chr.19:47354499 - 47522248 on Build GRCh38 | Loss | KPTN ZNF541 NAPA-AS1 NAPA SLC8A2 DHX34 MEIS3 |
nsv9738 | Chr.19:47356269 - 47427931 on Build GRCh38 | Gain | DHX34 MEIS3 |
More Information
Additional Information:
For this assay, SNP(s) [rs117534098] 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 |