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F8 c.98G>A ;(p.W33*)
Variant ID: X-154250730-C-T
NM_000132.3(
F8
):c.98G>A;(p.W33*)
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
The landscape of driver mutations in cutaneous squamous cell carcinoma.
Npj Genomic Medicine
Chang, Darwin D; Shain, A Hunter AH
Publication Date: 2021-07-16
Variant appearance in text: F8: W33*
PubMed Link:
34272401
Variant Present in the following documents:
41525_2021_226_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
A SINE Insertion in F8 Gene Leads to Severe Form of Hemophilia A in a Family of Rhodesian Ridgebacks.
Genes
Kehl, Alexandra A; Haaland, Anita Haug AH; Langbein-Detsch, Ines I; Mueller, Elisabeth E
Publication Date: 2021-01-21
Variant appearance in text: F8: Trp33*
PubMed Link:
33494213
Variant Present in the following documents:
Main text
genes-12-00134.pdf
View BVdb publication page
Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China.
Haemophilia : The Official Journal Of The World Federation Of Hemophilia
Feng, Yin Y; Li, Qianqian Q; Shi, Panlai P; Liu, Ning N; Kong, Xiangdong X; Guo, Ruixia R
Publication Date: 2021-01
Variant appearance in text: F8: 98G>A; Trp33Ter
PubMed Link:
33245802
Variant Present in the following documents:
View BVdb publication page
Canine and Feline Models of Human Genetic Diseases and Their Contributions to Advancing Clinical Therapies
.
The Yale Journal Of Biology And Medicine
Gurda, Brittney L BL; Bradbury, Allison M AM; Vite, Charles H CH
Publication Date: 2017-09
Variant appearance in text: F8: 98G>A
PubMed Link:
28955181
Variant Present in the following documents:
Main text
yjbm_90_3_417.pdf
View BVdb publication page