Bibliome.ai browser hg19
Search
About
Stats
FAQ
F8 c.274G>C ;(p.G92R)
Variant ID: X-154225362-C-G
NM_000132.3(
F8
):c.274G>C;(p.G92R)
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:
Mutational Profiles of F8 and F9 in a Cohort of Haemophilia A and Haemophilia B Patients in the Multi-ethnic Malaysian Population.
Mediterranean Journal Of Hematology And Infectious Diseases
Zahari, Maimiza M; Sulaiman, Siti Aishah SA; Othman, Zulhabri Z; Ayob, Yasmin Y; Karim, Faraizah Abd FA; Jamal, Rahman R
Publication Date: 2018
Variant appearance in text: F8: 274G>C; G92R
PubMed Link:
30210749
Variant Present in the following documents:
Main text
mjhid-10-1-e2018056.pdf
View BVdb publication page