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CYBB c.779C>T ;(p.P260L)
Variant ID: X-37658312-C-T
NM_000397.3(
CYBB
):c.779C>T;(p.P260L)
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:
Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype.
Archives Of Disease In Childhood
Dai, Dan D; Mei, Mei M; Hu, Liyuan L; Cao, Yun Y; Wang, Xiaochuan X; Wang, Libo L; Lu, Yulan Y; Yang, Lin L; Dong, Xinran X; Wang, Huijun H; Wu, Bingbing B; Qian, Liling L
Publication Date: 2022-02
Variant appearance in text: CYBB: P260L
PubMed Link:
34134972
Variant Present in the following documents:
archdischild-2021-322058supp001.pdf
View BVdb publication page