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F8 c.670+6T>C
Variant ID: X-154215506-A-G
NM_000132.3(
F8
):c.670+6T>C
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:
An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A.
Frontiers In Genetics
Balestra, Dario D; Maestri, Iva I; Branchini, Alessio A; Ferrarese, Mattia M; Bernardi, Francesco F; Pinotti, Mirko M
Publication Date: 2019
Variant appearance in text: FVIII: 670+6T>C
PubMed Link:
31649737
Variant Present in the following documents:
Main text
fgene-10-00974.pdf
View BVdb publication page