Variant NM_000492.4:c.571T>G
Name | NM_000492.4:c.571T>G |
Protein name | NP_000483.3:p.(Phe191Val) |
Genomic name (hg19) | chr7:g.117174411T>G UCSC |
#Exon/intron | exon 5 |
Legacy Name | F191V |
Class | disease-causing |
WT sequence | TCTCCTTTCCAACAACCTGAACAAA T TTGATGAAGTATGTACCTATTGATT |
Mutant sequence | TCTCCTTTCCAACAACCTGAACAAA G TTGATGAAGTATGTACCTATTGATT |
Not found | dbSNP rs141482808 |
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 |
clinical and functional data are provided by Vertex
No patient found in CFTR-NGS catalogue |
TOTAL NUMBER OF PATIENTS | 4 |
---|---|
CF | 1 |
CFTR-RD | 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) | 5359 | heterozygote | CF-causing - Trans |
CF | 5367 | heterozygote | CF-causing - Trans |
CBAVD | 2040 | heterozygote | varying clinical consequence- Undef |
Pancreatitis | 5611 | heterozygote | CFTR-RD-causing- Undef |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
CFTR variants are clustered into five groups: |
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