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CFTR-NGS variants catalogue
| Name | NM_000492.4:c.1210-34_1210-6TG[13]T[5] |
| #Exon/intron | intron 9 |
| Legacy Name | TG13T5 |
| Type in CFTR-NGS catalogue | repeat |
| Class in CFTR-France | disease-causing |
| Subclass | varying clinical consequence |
| MAF (GnomAD) | - |
| Splicing prediction (SpliceAI) | - |
 Not found |
 | dbSNP no rs |  Not found |  Not found |
| Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
| present | not performed |
