CFTR c.1585-9T>C

Variant ID: 7-117227784-T-C

NM_000492.3(CFTR):c.1585-9T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites.

American Journal Of Human Genetics
Lee, Melissa M; Roos, Patrick P; Sharma, Neeraj N; Atalar, Melis M; Evans, Taylor A TA; Pellicore, Matthew J MJ; Davis, Emily E; Lam, Anh-Thu N AN; Stanley, Susan E SE; Khalil, Sara E SE; Solomon, George M GM; Walker, Doug D; Raraigh, Karen S KS; Vecchio-Pagan, Briana B; Armanios, Mary M; Cutting, Garry R GR
Publication Date: 2017-05-04

Variant appearance in text: rs397508234
PubMed Link: 28475858
Variant Present in the following documents:
  • Main text
View BVdb publication page