Assay Details
Target Gene Details
Entrez Gene ID: | 55308 |
Gene Name: | DEAD-box helicase 19A |
Gene Aliases: |
DDX19-DDX19L, DDX19L |
Location: |
Chr.16:70346829-70373383 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DDX19A | NM_001320522.1 | 11 | 2143 | NP_001307451.1 |
NM_001320525.1 | 13 | 2297 | NP_001307454.1 | |
NM_001320526.1 | 12 | 2362 | NP_001307455.1 | |
NM_001320527.1 | 11 | 2252 | NP_001307456.1 | |
NM_018332.4 | 12 | 2236 | NP_060802.1 | |
NR_135296.1 | 10 | 2018 | ||
AB209401.1 | 5 | 4257 | BAD92638.1 | |
AK001988.1 | BAA92022.1 | |||
AK094061.1 | 2 | 1821 | ||
AL832901.1 | 8 | 1720 | CAH10629.1 | |
AL832970.1 | 12 | 2147 | CAH10622.1 | |
BC005162.2 | 12 | 2144 | AAH05162.1 | |
BC006544.2 | 12 | 2144 | AAH06544.1 | |
BC137496.1 | ||||
BC137497.1 | ||||
CR749227.1 | 12 | 2309 | CAH18083.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833272 | Chr.16:70335866 - 70535820 on Build GRCh38 | Loss | SNORD111B SF3B3 FUK COG4 LOC100506083 DDX19A ST3GAL2 |
More Information
Additional Information:
For this assay, SNP(s) [rs200206359] 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 |