Variant NM_000492.4:c.271G>A
| Name | NM_000492.4:c.271G>A |
| Protein name | NP_000483.3:p.(Gly91Arg) |
| Genomic name (hg19) | chr7:g.117149194G>A UCSC |
| Genomic name (hg38) | chr7:g.117509140G>A UCSC |
| #Exon/intron | exon 3 |
| Legacy Name | G91R |
| Class | disease-causing |
| Subclass | CF-causing |
| WT sequence | GTTCTATGGAATCTTTTTATATTTA G GGGTAAGGATCTCATTTGTACATTC |
| Mutant sequence | GTTCTATGGAATCTTTTTATATTTA A GGGTAAGGATCTCATTTGTACATTC |
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![]() | dbSNP rs121908750 |
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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 | 4 |
|---|---|
| CF | 4 |
| Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
| Phenotype | Patient ID | Variant status | Additional variants |
|---|---|---|---|
| CF | 3495 | heterozygote | CF-causing - Trans |
| CF | 3509 | heterozygote | CF-causing - Trans |
| CF | 3566 | heterozygote | CF-causing - Trans |
| CF | 3568 | heterozygote | CF-causing - Trans |
| 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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