catalog




CFTR-NGS variants catalogue



CFTR-NGS Variant details:
Name NM_000492.4:c.1210-34TG[13]
#Exon/intron intron 9
Legacy Name 1342-11TTT>G
Type in CFTR-NGS catalogue repeat
Class in CFTR-France non disease-causing


Additional information:
MAF (GnomAD) -
Splicing prediction (SpliceAI) -





External sources:

Not found		dbSNP
no rs
Not found
Not found

Variant validation:
Sanger
(present/not present/not verified)
 Minigene
(effect/no effect/not performed)
presentnot performed


No patient found in CFTR-NGS

3 individuals reported in CFTR-France







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