| 2024-10-14 | Class updated from VUS4 to unclassified /non-CF |
Variant NM_000492.4:c.1759T>A
| Name | NM_000492.4:c.1759T>A |
| Protein name | NP_000483.3:p.(Phe587Ile) |
| Genomic name (hg19) | chr7:g.117230486T>A UCSC |
| Genomic name (hg38) | chr7:g.117590432T>A UCSC |
| #Exon/intron | exon 13 |
| Legacy Name | F587I |
| Class | VUS |
| Subclass | non-CF |
| WT sequence | AGATGTTTTAACAGAAAAAGAAATA T TTGAAAGGTATGTTCTTTGAATACC |
| Mutant sequence | AGATGTTTTAACAGAAAAAGAAATA A TTGAAAGGTATGTTCTTTGAATACC |
![]() | ![]() Not found | dbSNP rs767349773 |
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| Modulator | FDA approval | EMA approval | in vitro / ex vivo data | clinical data |
| ELX-TEZ-IVA | yes | no | yes | no |
| VNZ-TEZ-DIVA | yes | no | yes | no |
clinical and functional data presented above are provided by Vertex
No patient found in CFTR-NGS catalogue |
| TOTAL NUMBER OF PATIENTS | 2 |
|---|---|
| CFTR-RD | 1
|
| Pending (NBS) | 1 |
| Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
| Phenotype | Patient ID | Variant status | Additional variants |
|---|---|---|---|
| Pending (NBS) | 5219 | heterozygote | CF-causing - Trans |
| CBAVD | 2681 | heterozygote | CF-causing- Undef |
| Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
| CFTR variants are clustered into five groups (click here for more details about the classification of variants): |
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