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CFTR-NGS variants catalogue
| Name | NM_000492.4:c.1680-877G>T |
| Protein name | NP_000483.3:p.(?) |
| Genomic name (hg19) | chr7:g.117229530G>T UCSC gnomAD |
| #Exon/intron | intron 12 |
| Legacy Name | 1811+1643G->T |
| Type in CFTR-NGS catalogue | - |
| Class in CFTR-France | disease-causing |
| Subclass | CF-causing |
| WT sequence | CCTATGTACTTGAGATATAAGTAAG G TTACTATCAATCACACCTGAAAAAT |
| Mutant sequence | CCTATGTACTTGAGATATAAGTAAG T TTACTATCAATCACACCTGAAAAAT |
| 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 |
