CFTR-NGS variants catalogue
Name | NM_000492.4:c.2645G>A |
Protein name | NP_000483.3:p.(Trp882*) |
Genomic name (hg19) | chr7:g.117242905G>A UCSC gnomAD |
#Exon/intron | exon 16 |
Legacy Name | W882X |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | disease-causing |
Subclass | CF-causing |
WT sequence | GTGGCTGCTTCTTTGGTTGTGCTGT G GCTCCTTGGAAAGTGAGTATTCCAT |
Mutant sequence | GTGGCTGCTTCTTTGGTTGTGCTGT A GCTCCTTGGAAAGTGAGTATTCCAT |
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 |