Variant NM_000492.4:c.416A>G
Name | NM_000492.4:c.416A>G |
Protein name | NP_000483.3:p.(His139Arg) |
Genomic name (hg19) | chr7:g.117171095A>G UCSC gnomAD |
#Exon/intron | exon 4 |
Legacy Name | H139R |
Class | disease-causing |
WT sequence | TTTATTGTGAGGACACTGCTCCTAC A CCCAGCCATTTTTGGCCTTCATCAC |
Mutant sequence | TTTATTGTGAGGACACTGCTCCTAC G CCCAGCCATTTTTGGCCTTCATCAC |
dbSNP rs76371115 |
Modulator | FDA approval | EMA approval | in vitro / ex vivo data | clinical data |
IVA | no | no | no | no |
TEZ-IVA | no | no | no | no |
ELX-TEZ-IVA | yes | no | yes | no |
clinical and functional data are provided by Vertex
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
No patient found in CFTR-NGS catalogue |
No patient found in CFTR-France |
CFTR variants are clustered into five groups: |
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