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F8 c.5292G>A ;(p.Q1764=)
Variant ID: X-154134776-C-T
NM_000132.3(
F8
):c.5292G>A;(p.Q1764=)
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:
Three novel F8 mutations in sporadic haemophilia A cases.
Springerplus
Hussain, Rashid R; Abid, Noman Bin NB; Hussain, Sajjad S; Shaukat, Zeeshan Z; Altaf, Mudassir M; Altaf, Sara S; Niazi, Gulzar G
Publication Date: 2012
Variant appearance in text: rs5986891
PubMed Link:
23961341
Variant Present in the following documents:
Main text
View BVdb publication page