Assay Details
Target Gene Details
Entrez Gene ID: | 10144 |
Gene Name: | family with sequence similarity 13 member A |
Gene Aliases: |
ARHGAP48, FAM13A1 |
Location: |
Chr.4:88725954-89111398 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 29 - Exon 30 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv470051 | Chr.4:88723780 - 89721993 on Build GRCh38 | Gain | FAM13A FAM13A-AS1 GPRIN3 TIGD2 |
nsv594806 | Chr.4:88621130 - 90539537 on Build GRCh38 | Gain | HERC3 MMRN1 SNCA FAM13A FAM13A-AS1 GPRIN3 SNCA-AS1 CCSER1 NAP1L5 TIGD2 |
More Information
Additional Information:
For this assay, SNP(s) [rs147595342] 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 Non-exonic DGV Variation |