Variant NM_000492.4:c.709C>G
Name | NM_000492.4:c.709C>G |
Protein name | NP_000483.3:p.(Gln237Glu) |
Genomic name (hg19) | chr7:g.117175431C>G UCSC |
#Exon/intron | exon 6 |
Legacy Name | Q237E |
Class | disease-causing |
Subclass | varying clinical consequence |
WT sequence | TTTCCTGATAGTCCTTGCCCTTTTT C AGGCTGGGCTAGGGAGAATGATGAT |
Mutant sequence | TTTCCTGATAGTCCTTGCCCTTTTT G AGGCTGGGCTAGGGAGAATGATGAT |
dbSNP rs397508784 |
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
No patient found in CFTR-NGS catalogue |
TOTAL NUMBER OF PATIENTS | 5 |
---|---|
Asymptomatic compound heterozygote | 1 |
CF | 3 |
Pending (NBS) | 1 |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
Phenotype | Patient ID | Variant status | Additional variants |
---|---|---|---|
CF | 559 | heterozygote | CF-causing - Trans |
CF | 4970 | heterozygote | CF-causing - Trans |
CF | 1894 | heterozygote | CF-causing - Trans |
Asymptomatic compound heterozygote | 5242 | heterozygote | varying clinical consequence- Undef |
Pending (NBS) | 5769 | heterozygote | CF-causing - Trans VUS3- Undef |
Color code: non disease-causing < likely benign < VUS < likely pathogenic < disease-causing |
CFTR variants are clustered into five groups: |
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