CFTR-NGS variants catalogue
Name | NM_000492.4:c.164+1G>C |
Protein name | NP_000483.3:p.(=) |
Genomic name (hg19) | chr7:g.117144418G>C UCSC gnomAD |
#Exon/intron | intron 2 |
Legacy Name | 296+1G>C |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | disease-causing |
Subclass | CF-causing |
WT sequence | ACAATCTATCTGAAAAATTGGAAAG G TATGTTCATGTACATTGTTTAGTTG |
Mutant sequence | ACAATCTATCTGAAAAATTGGAAAG C TATGTTCATGTACATTGTTTAGTTG |
MAF (GnomAD) | - |
Splicing prediction (SpliceAI) | - |
dbSNP no rs | Not found |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
present | not performed |