Assay Details
Target Gene Details
Entrez Gene ID: | 5909 |
Gene Name: | RAP1 GTPase activating protein |
Gene Aliases: |
RAP1GA1, RAP1GAP1, RAP1GAPII, RAPGAP |
Location: |
Chr.1:21596215-21669444 on Build GRCh38 |
Assay Gene Location: | Within Intron 21 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv428432 | Chr.1:21409691 - 21615921 on Build GRCh38 | Gain | RAP1GAP NBPF3 ALPL |
nsv834391 | Chr.1:21523440 - 21723989 on Build GRCh38 | Loss | USP48 RAP1GAP ALPL |
esv34155 | Chr.1:21367084 - 21840123 on Build GRCh38 | Loss | USP48 LDLRAD2 RAP1GAP HSPG2 NBPF3 ALPL |
nsv509002 | Chr.1:21578381 - 21654198 on Build GRCh38 | Insertion | RAP1GAP ALPL |
nsv470704 | Chr.1:21590741 - 21611881 on Build GRCh38 | Gain | RAP1GAP |
nsv954902 | Chr.1:21599708 - 21654507 on Build GRCh38 | Deletion | RAP1GAP |
nsv517096 | Chr.1:21537198 - 21670355 on Build GRCh38 | Loss | RAP1GAP ALPL |
nsv998678 | Chr.1:21564750 - 21614530 on Build GRCh38 | Gain | RAP1GAP ALPL |
More Information
Additional Information:
For this assay, SNP(s) [rs72660315] 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 |