Variant NM_000492.4:c.3017C>A
| Name | NM_000492.4:c.3017C>A |
| Protein name | NP_000483.3:p.(Ala1006Glu) |
| Genomic name (hg19) | chr7:g.117250601C>A UCSC |
| Genomic name (hg38) | chr7:g.117610547C>A UCSC |
| #Exon/intron | exon 19 |
| Legacy Name | A1006E |
| Class | disease-causing |
| Subclass | CF-causing |
| WT sequence | TTATTAATTGTGATTGGAGCTATAG C AGTTGTCGCAGTTTTACAACCCTAC |
| Mutant sequence | TTATTAATTGTGATTGGAGCTATAG A AGTTGTCGCAGTTTTACAACCCTAC |
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![]() | dbSNP rs397508480 |
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| Modulator | FDA approval | EMA approval | in vitro / ex vivo data | clinical data |
| IVA | no | no | no | no |
| TEZ-IVA | yes | no | yes | no |
| 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 |
|---|---|
| CF | 1 |
| CFTR-RD | 1
|
| Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
| Phenotype | Patient ID | Variant status | Additional variants |
|---|---|---|---|
| CF | 5374 | heterozygote | CFTR-RD-causing - Cis non-CF - Cis CF-causing - Trans |
| CBAVD | 6173 | heterozygote | varying clinical consequence- 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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