Variant NM_000492.4:c.2991G>C
Name | NM_000492.4:c.2991G>C |
Protein name | NP_000483.3:p.(Leu997Phe) |
Genomic name (hg19) | chr7:g.117250575G>C UCSC |
#Exon/intron | exon 19 |
Legacy Name | L997F |
Class | disease-causing |
Subclass | CFTR-RD-causing |
WT sequence | ACATGTTTTCTTTGATCTTACAGTT G TTATTAATTGTGATTGGAGCTATAG |
Mutant sequence | ACATGTTTTCTTTGATCTTACAGTT C TTATTAATTGTGATTGGAGCTATAG |
dbSNP rs1800111 |
Reference | PMID | Splicing | mRNA level | Maturation | Localization | Channel fonction (Cl-) | Bicarbonate |
Van Goor et al, 2014 | 23891399 | ✓ | ✓ | ✓ | |||
Sosnay et al, 2013 | 23974870 | ✓ | ✓ | ||||
LaRusch et al, 2014 | 25033378 | ✓ | ✓ | ✓ | |||
Bergougnoux et al, 2015 | 25797027 | ✓ | ✓ | ✓ |
« ✓ » indicates the type of analysis performed and not the results
Modulator | FDA approval | EMA approval | in vitro / ex vivo data | clinical data |
IVA | yes | no | yes | no |
TEZ-IVA | yes | no | yes | no |
ELX-TEZ-IVA | yes | no | yes | no |
clinical and functional data are provided by Vertex
4 individuals carrying this variant are reported in CFTR-NGS catalogue |
TOTAL NUMBER OF PATIENTS | 117 |
---|---|
Asymptomatic compound heterozygote | 10 |
CF | 4 |
CFTR-RD | 90
|
Fetal bowel anomalies | 1 |
Pending | 2 |
Pending (NBS) | 10 |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
Phenotype | Patient ID | Variant status | Additional variants |
---|---|---|---|
Pancreatitis | 5368 | heterozygote | varying clinical consequence- Undef |
Pancreatitis | 2242 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef CFTR-RD-causing- Undef |
Pancreatitis | 2285 | heterozygote | |
Pancreatitis | 2346 | heterozygote | CF-causing- Undef |
Pancreatitis | 2483 | heterozygote | |
Pancreatitis | 2486 | heterozygote | VUS3- Undef non-CF- Undef |
Pancreatitis | 4918 | heterozygote | VUS3- Undef |
Pancreatitis | 2198 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 5388 | heterozygote | |
Pancreatitis | 5453 | heterozygote | CF-causing- Undef |
Pancreatitis | 5454 | heterozygote | CF-causing- Undef |
Pancreatitis | 5455 | heterozygote | CF-causing- Undef |
Pancreatitis | 5668 | heterozygote | CF-causing- Undef |
Pancreatitis | 5700 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 5870 | heterozygote | VUS3- Undef non-CF- Undef |
Pancreatitis | 5879 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 5894 | heterozygote | VUS3- Undef |
Pancreatitis | 2748 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 2785 | heterozygote | |
Pancreatitis | 5623 | heterozygote | CFTR-RD-causing - Trans CFTR-RD-causing - Trans CFTR-RD-causing - Trans |
Pancreatitis | 4318 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 5010 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 2786 | heterozygote | CF-causing - Trans |
Pancreatitis | 3182 | heterozygote | CF-causing- Undef |
Pancreatitis | 3312 | heterozygote | |
Pancreatitis | 5102 | heterozygote | |
Pancreatitis | 76 | heterozygote | CF-causing - Trans |
Pancreatitis | 964 | heterozygote | VUS3 - Trans |
Pancreatitis | 1650 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 4977 | heterozygote | CF-causing- Undef |
Pancreatitis | 1836 | heterozygote | CF-causing- Undef |
Pancreatitis | 5145 | heterozygote | CF-causing- Undef |
Pancreatitis | 4926 | homozygote | c.2991G>C - p.(Leu997Phe) - Trans |
Pancreatitis | 5125 | homozygote | c.2991G>C - p.(Leu997Phe) - Trans |
Pancreatitis | 6204 | homozygote | c.2991G>C - p.(Leu997Phe) - Trans |
Pancreatitis | 5862 | homozygote | c.2991G>C - p.(Leu997Phe) - Trans |
Pending (NBS) | 2038 | heterozygote | CF-causing- Undef |
Pending (NBS) | 6017 | heterozygote | |
Pending (NBS) | 6003 | heterozygote | CF-causing- Undef |
Pending (NBS) | 6084 | heterozygote | CF-causing- Undef |
Pending (NBS) | 6089 | heterozygote | |
Pending (NBS) | 4666 | heterozygote | CF-causing - Trans |
Pending (NBS) | 4693 | heterozygote | CF-causing - Trans |
Pending (NBS) | 4667 | heterozygote | CF-causing - Trans |
Pending (NBS) | 352 | heterozygote | CF-causing - Trans |
Pending (NBS) | 5183 | heterozygote | CF-causing - Trans VUS3- Undef |
Bronchiectasis | 2367 | heterozygote | |
Bronchiectasis | 4906 | heterozygote | CFTR-RD-causing - Trans |
Bronchiectasis | 1985 | heterozygote | CF-causing- Undef |
Bronchiectasis | 4613 | heterozygote | |
Bronchiectasis | 3213 | heterozygote | CF-causing - Cis varying clinical consequence - Trans |
Bronchiectasis | 560 | heterozygote | CF-causing- Undef |
Bronchiectasis | 4726 | heterozygote | varying clinical consequence- Undef |
Bronchiectasis | 4866 | heterozygote | CF-causing- Undef |
Bronchiectasis | 5153 | homozygote | c.2991G>C - p.(Leu997Phe) - Trans |
Other | 2696 | heterozygote | varying clinical consequence- Undef |
Other | 4582 | heterozygote | CF-causing- Undef |
Other | 4664 | heterozygote | CF-causing- Undef |
Other | 645 | heterozygote | CF-causing- Undef |
Other | 4842 | heterozygote | VUS3 - Trans |
Other | 5201 | heterozygote | CF-causing- Undef |
CBAVD | 4905 | heterozygote | CF-causing- Undef |
CBAVD | 4919 | heterozygote | CF-causing- Undef |
CBAVD | 2689 | heterozygote | CF-causing- Undef |
CBAVD | 5444 | heterozygote | CF-causing- Undef |
CBAVD | 5871 | heterozygote | CF-causing- Undef |
CBAVD | 4586 | heterozygote | |
CBAVD | 4589 | heterozygote | |
CBAVD | 3318 | heterozygote | VUS3 - Trans non-CF - Trans |
CBAVD | 3361 | heterozygote | CF-causing- Undef |
CBAVD | 3366 | heterozygote | CF-causing- Undef |
CBAVD | 3377 | heterozygote | CF-causing - Trans |
CBAVD | 513 | heterozygote | CF-causing - Trans |
CBAVD | 525 | heterozygote | CF-causing - Trans |
CBAVD | 538 | heterozygote | CFTR-RD-causing - Trans CFTR-RD-causing - Trans |
CBAVD | 707 | heterozygote | |
CBAVD | 736 | heterozygote | CF-causing- Undef |
CBAVD | 849 | heterozygote | CF-causing- Undef |
CBAVD | 510 | heterozygote | |
CBAVD | 489 | heterozygote | CFTR-RD-causing - Trans |
CBAVD | 428 | heterozygote | CF-causing - Trans |
CBAVD | 447 | heterozygote | CF-causing- Undef |
CBAVD | 461 | heterozygote | CF-causing- Undef |
CBAVD | 462 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 469 | heterozygote | CF-causing- Undef |
CBAVD | 482 | heterozygote | |
CBAVD | 483 | heterozygote | CF-causing- Undef |
CBAVD | 981 | heterozygote | CFTR-RD-causing- Undef |
CBAVD | 1464 | heterozygote | VUS3 - Trans non-CF - Trans |
CBAVD | 1487 | heterozygote | CF-causing- Undef |
CBAVD | 1634 | heterozygote | CF-causing- Undef |
CBAVD | 1655 | heterozygote | CF-causing- Undef |
CBAVD | 1759 | heterozygote | CF-causing- Undef |
CBAVD | 1294 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5819 | heterozygote | CF-causing- Undef |
Asymptomatic compound heterozygote | 4749 | heterozygote | CF-causing - Trans |
Asymptomatic compound heterozygote | 3235 | heterozygote | VUS3 - Trans |
Asymptomatic compound heterozygote | 558 | heterozygote | CF-causing - Trans |
Asymptomatic compound heterozygote | 575 | heterozygote | CFTR-RD-causing - Trans |
Asymptomatic compound heterozygote | 740 | heterozygote | CFTR-RD-causing - Trans CFTR-RD-causing - Trans |
Asymptomatic compound heterozygote | 965 | heterozygote | VUS3 - Trans |
Asymptomatic compound heterozygote | 4960 | heterozygote | |
Asymptomatic compound heterozygote | 5222 | heterozygote | VUS3- Undef |
Asymptomatic compound heterozygote | 5815 | heterozygote | |
Asymptomatic compound heterozygote | 739 | homozygote | c.2991G>C - p.(Leu997Phe) - Trans |
Fetal bowel anomalies | 828 | heterozygote | CF-causing - Trans |
Aquagenic palmoplantar keratoderma | 4827 | heterozygote | CF-causing- Undef |
Aquagenic palmoplantar keratoderma | 5470 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef CFTR-RD-causing- Undef |
CF | 5993 | heterozygote | CFTR-RD-causing - Cis CFTR-RD-causing - Cis CF-causing - Trans |
CF | 5026 | heterozygote | CF-causing - Trans |
CF | 4962 | heterozygote | CF-causing - Trans |
CF | 4790 | heterozygote | CF-causing- Undef |
Pending | 1240 | heterozygote | |
Pending | 4748 | heterozygote | CF-causing - Trans |
CRS-NP | 5778 | heterozygote | VUS3- Undef |
CRS-NP | 5338 | heterozygote | non-CF- Undef |
CRS-NP | 5994 | heterozygote | CFTR-RD-causing - Cis CFTR-RD-causing - Cis CF-causing - Trans |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
CFTR variants are clustered into five groups: |
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