Variant NM_000492.4:c.2909-92G>A
Name | NM_000492.4:c.2909-92G>A |
Protein name | NP_000483.3:p.(=) |
Genomic name (hg19) | chr7:g.117246636G>A UCSC |
#Exon/intron | intron 17 |
Legacy Name | 3041-92G/A |
Class | non disease-causing |
WT sequence | TAATTCTTATTTGGGTTCTGAATGC G TCTACTGTGATCCAAACTTAGTATT |
Mutant sequence | TAATTCTTATTTGGGTTCTGAATGC A TCTACTGTGATCCAAACTTAGTATT |
Not found | dbSNP rs35050470 |
Not found |
55 individuals carrying this variant are reported in CFTR-NGS catalogue |
TOTAL NUMBER OF PATIENTS | 189 |
---|---|
Asymptomatic compound heterozygote | 16 |
CF | 34 |
CFTR-RD | 120
|
Pending | 1 |
Pending (NBS) | 16 |
Pending non-CF | 2 |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
Phenotype | Patient ID | Variant status | Additional variants |
---|---|---|---|
CF | 4629 | heterozygote | CF-causing- Undef CF-causing- Undef VUS1- Undef |
CF | 4765 | heterozygote | VUS3- Undef varying clinical consequence- Undef CF-causing- Undef |
CF | 5016 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 5807 | heterozygote | CF-causing- Undef VUS3- Undef |
CF | 5215 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef CFTR-RD-causing- Undef |
CF | 5622 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 5777 | heterozygote | VUS3- Undef CF-causing- Undef VUS3- Undef |
CF | 5965 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 5948 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 5345 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 5341 | heterozygote | VUS3- Undef CF-causing- Undef |
CF | 5328 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 5174 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 663 | heterozygote | VUS2- Undef CF-causing- Undef varying clinical consequence- Undef |
CF | 662 | heterozygote | VUS2- Undef CF-causing- Undef varying clinical consequence- Undef |
CF | 654 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 745 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 4697 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 383 | heterozygote | varying clinical consequence- Undef CF-causing- Undef CF-causing- Undef |
CF | 316 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 4665 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
CF | 909 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 920 | heterozygote | VUS2- Undef CF-causing- Undef CF-causing- Undef |
CF | 947 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 945 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 808 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CF | 816 | heterozygote | CF-causing- Undef CF-causing- Undef |
CF | 829 | heterozygote | CF-causing- Undef varying clinical consequence- Undef VUS3- Undef |
CF | 730 | homozygote | c.3131A>G - p.(Glu1044Gly) - Trans |
CF | 4718 | homozygote | c.2374C>T - p.(Arg792*) - Trans c.870-1113_870-1110del - p.(=) - Trans |
CF | 4688 | homozygote | c.1519_1521del - p.(Ile507del) - Trans c.2657+5G>A - p.(=) - Trans |
CF | 5069 | homozygote | c.1393-1G>A - p.(=) - Trans c.1680-981T>C - p.(=) - Trans c.3874-4522A>G - p.(=) - Trans |
CF | 882 | homozygote | c.1518C>G - p.(Ile506Met) - Trans c.1521_1523del - p.(Phe508del) - Trans |
CF | 901 | homozygote | c.2657+5G>A - p.(=) - Trans |
Other | 4625 | heterozygote | VUS3- Undef |
Other | 5224 | heterozygote | VUS3- Undef VUS3- Undef |
Other | 5743 | heterozygote | CF-causing- Undef VUS3- Undef CFTR-RD-causing- Undef |
Other | 4760 | heterozygote | VUS3- Undef |
Other | 5575 | heterozygote | VUS3- Undef CF-causing- Undef |
Other | 5825 | heterozygote | VUS3- Undef CF-causing- Undef |
Other | 5823 | heterozygote | VUS3- Undef CF-causing- Undef non-CF- Undef VUS3- Undef |
Other | 5967 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Other | 5763 | heterozygote | VUS3- Undef CF-causing- Undef non-CF- Undef |
Other | 4686 | heterozygote | VUS3- Undef CF-causing- Undef |
Other | 4671 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
Other | 4835 | heterozygote | CFTR-RD-causing- Undef VUS3- Undef |
Other | 5083 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef CF-causing- Undef |
Other | 4826 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
Other | 972 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
Other | 940 | heterozygote | CF-causing- Undef |
Other | 935 | heterozygote | CFTR-RD-causing- Undef |
Other | 5087 | heterozygote | VUS3- Undef VUS3- Undef |
Other | 5082 | homozygote | c.1116+1G>A - p.(=) - Trans c.1210-34_1210-6TG[11]T[5] - Trans |
CBAVD | 5173 | heterozygote | CF-causing- Undef varying clinical consequence- Undef VUS3- Undef |
CBAVD | 3267 | heterozygote | VUS3- Undef CF-causing- Undef |
CBAVD | 3125 | heterozygote | CF-causing- Undef VUS1- Undef varying clinical consequence- Undef |
CBAVD | 5330 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 4752 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5228 | heterozygote | CFTR-RD-causing- Undef VUS3- Undef |
CBAVD | 5600 | heterozygote | VUS3- Undef |
CBAVD | 4756 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 4651 | heterozygote | VUS3- Undef CF-causing- Undef VUS1- Undef |
CBAVD | 4653 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef |
CBAVD | 1276 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
CBAVD | 5821 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 5768 | heterozygote | CF-causing- Undef VUS3- Undef |
CBAVD | 5947 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5943 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5764 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5944 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5591 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef |
CBAVD | 5590 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5346 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 5343 | heterozygote | VUS3- Undef VUS3- Undef |
CBAVD | 5314 | heterozygote | VUS3- Undef CF-causing- Undef |
CBAVD | 765 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 664 | heterozygote | |
CBAVD | 659 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef VUS3- Undef |
CBAVD | 658 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 656 | heterozygote | varying clinical consequence- Undef CF-causing- Undef |
CBAVD | 653 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef varying clinical consequence- Undef |
CBAVD | 665 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
CBAVD | 676 | heterozygote | VUS3- Undef |
CBAVD | 763 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 743 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
CBAVD | 735 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
CBAVD | 720 | heterozygote | CFTR-RD-causing- Undef |
CBAVD | 710 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 690 | heterozygote | |
CBAVD | 682 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 643 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef |
CBAVD | 423 | heterozygote | VUS3- Undef |
CBAVD | 4706 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 4683 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 4679 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 4735 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef varying clinical consequence- Undef |
CBAVD | 5072 | heterozygote | CF-causing- Undef VUS3- Undef |
CBAVD | 4837 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef |
CBAVD | 900 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 892 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef CFTR-RD-causing- Undef CFTR-RD-causing- Undef |
CBAVD | 887 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
CBAVD | 858 | heterozygote | |
CBAVD | 857 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 856 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
CBAVD | 912 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 949 | heterozygote | VUS3- Undef CF-causing- Undef |
CBAVD | 941 | heterozygote | VUS4- Undef CF-causing- Undef |
CBAVD | 840 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 805 | heterozygote | VUS1- Undef |
CBAVD | 781 | heterozygote | VUS3- Undef |
CBAVD | 812 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
CBAVD | 818 | heterozygote | |
CBAVD | 834 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
CBAVD | 725 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.1684G>A - p.(Val562Ile) - Trans c.3846G>A - p.(Trp1282*) - Trans |
CBAVD | 881 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.617T>G - p.(Leu206Trp) - Trans |
CBAVD | 5592 | homozygote | c.1210-34_1210-6TG[12]T[5] - Trans c.233dup - p.(Trp79Leufs*32) - Trans |
CBAVD | 908 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.1466C>T - p.(Ser489Leu) - Trans c.1684G>A - p.(Val562Ile) - Trans |
CBAVD | 919 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.1684G>A - p.(Val562Ile) - Trans c.3846G>A - p.(Trp1282*) - Trans |
CBAVD | 5610 | homozygote | c.1327G>T - p.(Asp443Tyr) - Trans c.1521_1523del - p.(Phe508del) - Trans c.2002C>T - p.(Arg668Cys) - Trans |
CBAVD | 5129 | homozygote | c.1519_1521del - p.(Ile507del) - Trans c.1704G>T - p.(Leu568Phe) - Trans |
Pancreatitis | 4619 | heterozygote | VUS3- Undef VUS3- Undef |
Pancreatitis | 4659 | heterozygote | VUS3- Undef |
Pancreatitis | 5621 | heterozygote | CFTR-RD-causing- Undef |
Pancreatitis | 5619 | heterozygote | VUS3- Undef |
Pancreatitis | 5614 | heterozygote | VUS3- Undef |
Pancreatitis | 5605 | heterozygote | VUS2- Undef |
Pancreatitis | 5977 | heterozygote | VUS3- Undef |
Pancreatitis | 5364 | heterozygote | VUS3- Undef |
Pancreatitis | 5340 | heterozygote | CFTR-RD-causing- Undef VUS3- Undef |
Pancreatitis | 5336 | heterozygote | VUS3- Undef VUS3- Undef |
Pancreatitis | 5329 | heterozygote | varying clinical consequence- Undef |
Pancreatitis | 5155 | heterozygote | CFTR-RD-causing- Undef VUS3- Undef VUS3- Undef |
Pancreatitis | 5171 | heterozygote | VUS3- Undef VUS3- Undef |
Pancreatitis | 648 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef |
Pancreatitis | 4708 | heterozygote | VUS3- Undef VUS3- Undef |
Pancreatitis | 3259 | heterozygote | varying clinical consequence- Undef CF-causing- Undef |
Bronchiectasis | 4657 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Bronchiectasis | 5530 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
Bronchiectasis | 5624 | heterozygote | VUS3- Undef CF-causing- Undef |
Bronchiectasis | 693 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef VUS1- Undef |
Bronchiectasis | 4726 | heterozygote | CFTR-RD-causing- Undef varying clinical consequence- Undef |
Bronchiectasis | 4725 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
Bronchiectasis | 5074 | heterozygote | VUS3 - Cis VUS3 - Trans |
Bronchiectasis | 966 | homozygote | c.1585-9418T>C - p.(=) - Trans c.899C>A - p.(Ala300Asp) - Trans |
Bronchiectasis | 5972 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.870-1113_870-1110del - p.(=) - Trans |
Bronchiectasis | 777 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.1684G>A - p.(Val562Ile) - Trans |
Bronchiectasis | 5126 | homozygote | c.1327G>T - p.(Asp443Tyr) - Trans c.2002C>T - p.(Arg668Cys) - Trans |
Bronchiectasis | 5076 | homozygote | c.2658-77T>A - p.(=) - Trans |
Asymptomatic compound heterozygote | 4617 | heterozygote | VUS3 - Cis CF-causing - Trans |
Asymptomatic compound heterozygote | 4628 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
Asymptomatic compound heterozygote | 4763 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
Asymptomatic compound heterozygote | 5525 | heterozygote | VUS3- Undef VUS3- Undef |
Asymptomatic compound heterozygote | 5220 | heterozygote | VUS3- Undef non-CF- Undef |
Asymptomatic compound heterozygote | 5362 | heterozygote | VUS3- Undef VUS3- Undef |
Asymptomatic compound heterozygote | 5606 | heterozygote | VUS3- Undef non-CF- Undef CF-causing- Undef |
Asymptomatic compound heterozygote | 5602 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef VUS3- Undef |
Asymptomatic compound heterozygote | 5601 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
Asymptomatic compound heterozygote | 5964 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef CFTR-RD-causing- Undef |
Asymptomatic compound heterozygote | 5167 | heterozygote | varying clinical consequence- Undef |
Asymptomatic compound heterozygote | 5077 | heterozygote | VUS3- Undef CFTR-RD-causing- Undef |
Asymptomatic compound heterozygote | 5073 | heterozygote | CFTR-RD-causing- Undef |
Asymptomatic compound heterozygote | 4741 | homozygote | c.3154T>G - p.(Phe1052Val) - Trans c.489+3A>G - p.(=) - Trans |
Asymptomatic compound heterozygote | 5218 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.2758G>T - p.(Val920Leu) - Trans c.3409A>G - p.(Met1137Val) - Trans |
Asymptomatic compound heterozygote | 5745 | homozygote | c.1210-34_1210-6TG[11]T[5] - Trans c.3256A>G - p.(Thr1086Ala) - Trans |
Pending (NBS) | 4643 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
Pending (NBS) | 5017 | heterozygote | CF-causing- Undef CFTR-RD-causing- Undef |
Pending (NBS) | 4631 | heterozygote | varying clinical consequence- Undef CF-causing- Undef |
Pending (NBS) | 4645 | heterozygote | CF-causing- Undef VUS3- Undef |
Pending (NBS) | 4654 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Pending (NBS) | 5247 | heterozygote | VUS3- Undef VUS3- Undef CF-causing- Undef VUS1- Undef |
Pending (NBS) | 5808 | heterozygote | CF-causing- Undef VUS3- Undef |
Pending (NBS) | 5609 | heterozygote | VUS3- Undef CF-causing- Undef |
Pending (NBS) | 5951 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Pending (NBS) | 5769 | heterozygote | CF-causing- Undef varying clinical consequence- Undef VUS3- Undef |
Pending (NBS) | 5342 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Pending (NBS) | 387 | heterozygote | CF-causing- Undef VUS3- Undef |
Pending (NBS) | 803 | heterozygote | VUS2- Undef CF-causing- Undef |
Pending (NBS) | 799 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Pending (NBS) | 794 | heterozygote | CF-causing- Undef varying clinical consequence- Undef |
Pending (NBS) | 4644 | homozygote | c.1209G>C - p.(Glu403Asp) - Trans c.2657+5G>A - p.(=) - Trans |
Pending non-CF | 4825 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef varying clinical consequence- Undef |
Pending non-CF | 5009 | heterozygote | VUS3- Undef CF-causing- Undef |
CRS-NP | 5138 | heterozygote | CFTR-RD-causing- Undef VUS3- Undef |
CRS-NP | 3161 | heterozygote | CF-causing- Undef VUS1- Undef varying clinical consequence- Undef |
Aquagenic palmoplantar keratoderma | 5149 | heterozygote | VUS3- Undef CF-causing- Undef |
Aquagenic palmoplantar keratoderma | 5613 | heterozygote | non-CF- Undef |
Aquagenic palmoplantar keratoderma | 4660 | homozygote | c.2002C>T - p.(Arg668Cys) - Trans c.2657+5G>A - p.(=) - Trans |
Aquagenic palmoplantar keratoderma | 5772 | homozygote | c.4139C>T - p.(Thr1380Ile) - Trans |
Pending | 5008 | heterozygote | varying clinical consequence- Undef CF-causing- Undef |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
CFTR variants are clustered into five groups: |
|