CFTR-NGS variants catalogue
Variant hg19:chr7:117240175G/A
Name | NM_000492.4:c.2620-2705G>A |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117240175G>A UCSC gnomAD |
#Exon/intron | intron 15 |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | not reported |
WT sequence | TAGTCTTTTAAAAAATTTCTTCAAA G CTATTAAACTGAAAAAAAATTAATT |
Mutant sequence | TAGTCTTTTAAAAAATTTCTTCAAA A CTATTAAACTGAAAAAAAATTAATT |
MAF (GnomAD) | 1.06e-02 |
Splicing prediction (SpliceAI) | AG: 0.00 (38) AL: 0.00 (1) DG: 0.00 (-27) DL: 0.00 (1) |
![]() Not found | ![]() Not found | dbSNP rs79911188 | ![]() Not found | ![]() |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
not verified | not performed |
No patient found in CFTR-France |
TOTAL NUMBER OF INDIVIDUALS | 1 |
---|---|
Suspicion of CF | 1 |