CFTR-NGS variants catalogue
Name | NM_000492.4:c.1397C>G |
Protein name | NP_000483.3:p.(Ser466*) |
Genomic name (hg19) | chr7:g.117199522C>G UCSC gnomAD |
#Exon/intron | exon 11 |
Legacy Name | S466X(TAG) |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | disease-causing |
Subclass | CF-causing |
WT sequence | AATGATGGGTTTTATTTCCAGACTT C ACTTCTAATGGTGATTATGGGAGAA |
Mutant sequence | AATGATGGGTTTTATTTCCAGACTT G ACTTCTAATGGTGATTATGGGAGAA |
MAF (GnomAD) | - |
Splicing prediction (SpliceAI) | - |
dbSNP no rs | Not found |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
present | not performed |