F8 c.*1475C>T

Variant ID: X-154064397-G-A

NM_000132.3(F8):c.*1475C>T

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:

In silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B.

Journal Of Biomedical Science
Doss C, George Priya GP
Publication Date: 2012-03-16

Variant appearance in text: rs34683807
PubMed Link: 22423892
Variant Present in the following documents:
  • Main text
  • 1423-0127-19-30.pdf
View BVdb publication page