CFTR-NGS variants catalogue
Name | NM_000492.4:c.3468+2T>C |
Protein name | NP_000483.3:p.(=) |
Genomic name (hg19) | chr7:g.117254769T>C UCSC gnomAD |
#Exon/intron | intron 21 |
Legacy Name | 3600+2T>C |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | disease-causing |
Subclass | CF-causing |
WT sequence | TCCAGCATAGATGTGGATAGCTTGG T AAGTCTTATCATCTTTTTAACTTTT |
Mutant sequence | TCCAGCATAGATGTGGATAGCTTGG C AAGTCTTATCATCTTTTTAACTTTT |
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 |