Bibliome.ai browser hg19
Search
About
Stats
FAQ
F8 c.1996_1997delinsAT ;(p.D666I)
Variant ID: X-154176089-TC-AT
NM_000132.3(
F8
):c.1996_1997delinsAT;(p.D666I)
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:
Role of hydrophobic mutations on the binding affinity and stability of blood coagulation factor VIIIa: a computational molecular dynamics and free-energy analysis.
Biochemical And Biophysical Research Communications
Venkateswarlu, Divi D
Publication Date: 2014-07-18
Variant appearance in text: FVIII: D666I
PubMed Link:
24952158
Variant Present in the following documents:
Main text
View BVdb publication page