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F8 c.6429+1G>A
Variant ID: X-154124351-C-T
NM_000132.3(
F8
):c.6429+1G>A
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:
Bioengineering hemophilia A-specific microvascular grafts for delivery of full-length factor VIII into the bloodstream.
Blood Advances
Neumeyer, Joseph J; Lin, Ruei-Zeng RZ; Wang, Kai K; Hong, Xuechong X; Hua, Tien T; Croteau, Stacy E SE; Neufeld, Ellis J EJ; Melero-Martin, Juan M JM
Publication Date: 2019-12-23
Variant appearance in text: F8: 6429+1G>A
PubMed Link:
31851760
Variant Present in the following documents:
Main text
View BVdb publication page