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CFTR c.169T>A ;(p.W57R)
Variant ID: 7-117149092-T-A
NM_000492.3(
CFTR
):c.169T>A;(p.W57R)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
Orphanet Journal Of Rare Diseases
De Wachter, E E; Thomas, M M; Wanyama, S S SS; Seneca, S S; Malfroot, A A
Publication Date: 2017-08-22
Variant appearance in text: CFTR: W57R
PubMed Link:
28830496
Variant Present in the following documents:
Main text
13023_2017_Article_694.pdf
View BVdb publication page