CFTR-NGS variants catalogue
Name | NM_000492.4:c.2044dup |
Protein name | NP_000483.3:p.(Thr682Asnfs*7) |
Genomic name (hg19) | chr7:g.117232265dup UCSC |
#Exon/intron | exon 14 |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | disease-causing |
WT sequence | GATGCTCCTGTCTCCTGGACAGAAA - CAAAAAAACAATCTTTTAAACAGAC |
Mutant sequence | GATGCTCCTGTCTCCTGGACAGAAA A CAAAAAAACAATCTTTTAAACAGAC |
MAF (GnomAD) | - |
Splicing prediction (SpliceAI) | - |
Not found | dbSNP no rs | Not found |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
present | not performed |
No patient found in CFTR-NGS |
No patient found in CFTR-France |