CFTR-NGS variants catalogue
Name | NM_000492.4:c.3874-1_3874delinsAG |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117292895_117292896delinsAG UCSC |
#Exon/intron | intron 23 |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | disease-causing |
WT sequence | TCTTCTTCTTTTCTTTTTTGCTATA GA AAGTATTTATTTTTTCTGGAACATT |
Mutant sequence | TCTTCTTCTTTTCTTTTTTGCTATA AG AAGTATTTATTTTTTCTGGAACATT |
MAF (GnomAD) | - |
Splicing prediction (SpliceAI) | - |
Not found | Not found | dbSNP no rs | Not found |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
present | not performed |