| 2018-03-09 | class changed from unclassified to disease-causing |
Variant NM_000492.4:c.1811C>T
| Name | NM_000492.4:c.1811C>T |
| Protein name | NP_000483.3:p.(Thr604Ile) |
| Genomic name (hg19) | chr7:g.117232032C>T UCSC |
| Genomic name (hg38) | chr7:g.117591978C>T UCSC |
| #Exon/intron | exon 14 |
| Legacy Name | T604I |
| Class | disease-causing |
| WT sequence | GCTAACAAAACTAGGATTTTGGTCA C TTCTAAAATGGAACATTTAAAGAAA |
| Mutant sequence | GCTAACAAAACTAGGATTTTGGTCA T TTCTAAAATGGAACATTTAAAGAAA |
![]() | ![]() Not found | dbSNP rs397508308 |
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| Modulator | FDA approval | EMA approval | in vitro / ex vivo data | clinical data |
| 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 | 3 |
|---|---|
| CF | 2 |
| Pending (NBS) | 1 |
| Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
| Phenotype | Patient ID | Variant status | Additional variants |
|---|---|---|---|
| Pending (NBS) | 1563 | heterozygote | CF-causing - Trans |
| CF | 1757 | heterozygote | CF-causing- Undef |
| CF | 1758 | 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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