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CFTR-NGS variants catalogue
| Name | NM_000492.4:c.3717+1G>A |
| Protein name | NP_000483.3:p.(=) |
| Genomic name (hg19) | chr7:g.117267825G>A UCSC gnomAD |
| #Exon/intron | intron 22 |
| Legacy Name | 3849+ 1G- >A |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | disease-causing |
| Subclass | CF-causing |
| WT sequence | CTTCTCAATAAGTCCTGGCCAGAGG G TGAGATTTGAACACTGCTTGCTTTG |
| Mutant sequence | CTTCTCAATAAGTCCTGGCCAGAGG A TGAGATTTGAACACTGCTTGCTTTG |
| 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 |
