PGLNext®
| Test Code | 5504 |
| Turnaround Time (TAT) | 14-21 days |
| Number of Genes | 12 |
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- Order a Sample Kit
We offer family variant testing at no additional cost
for all blood relatives of patients who undergo full single gene sequencing or multigene panel testing* at Ambry Genetics and are found to have a pathogenic or likely pathogenic variant. No-cost testing of blood relatives must be completed within 90 days of the original Ambry report date.
Order Now*excludes Secondary Findings and SNP Array tests
When To Consider Testing
- PGL/PCC at any age
- Presence of PGL/PCC with a personal or family history* of kidney, thyroid, or breast cancer
- Presence of PGL/PCC with a personal or family history* of neurofibromas, kidney, or gastrointestinal stromal tumors (GIST)
* On the same side of the family
Mutation Detection Rate
PGLNext can detect >99.9% of described mutations in the included genes, when present (analytic sensitivity).
Test Description
PGLNext analyzes 12 genes (listed above). All genes are evaluated by next generation sequencing (NGS) or Sanger sequencing of all coding domains, and well into the flanking 5’ and 3’ ends of all the introns and untranslated regions. Clinically significant intronic findings beyond 5 base pairs are always reported. Intronic variants of unknown or unlikely clinical significance are not reported beyond 5 base pairs from the splice junction. Additional Sanger sequencing is performed for any regions missing or with insufficient read depth coverage for reliable heterozygous variant detection. Potentially homozygous variants, variants in regions complicated by pseudogene interference, and variant calls not satisfying depth of coverage and variant allele frequency quality thresholds are verified by Sanger sequencing. Gross deletion/duplication analysis is performed for the covered exons and untranslated regions of all 12 genes using read-depth from NGS data with confirmatory multiplex ligation-dependent probe amplification (MLPA) and/or targeted chromosomal microarray.