EGF c.314_315delinsAC ;(p.G105D)

Variant ID: 4-110862288-GG-AC

NM_001963.4(EGF):c.314_315delinsAC;(p.G105D)

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 analysis of missense mutations in exons 1-5 of the F9 gene that cause hemophilia B.

Bmc Bioinformatics
Meléndez-Aranda, Lennon L; Jaloma-Cruz, Ana Rebeca AR; Pastor, Nina N; Romero-Prado, Marina María de Jesús MMJ
Publication Date: 2019-06-28

Variant appearance in text: EGF: Gly105Asp
PubMed Link: 31253089
Variant Present in the following documents:
  • Main text
  • 12859_2019_Article_2919.pdf
View BVdb publication page