GC c.1098dup ;(p.P367Afs*8)

Variant ID: 4-72620760-G-GC

NM_000583.3(GC):c.1098dup;(p.P367Afs*8)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Haplotype-resolved de novo assembly of the Vero cell line genome.

Npj Vaccines
Sène, Marie-Angélique MA; Kiesslich, Sascha S; Djambazian, Haig H; Ragoussis, Jiannis J; Xia, Yu Y; Kamen, Amine A AA
Publication Date: 2021-08-20

Variant appearance in text: GC: 1098dupG
PubMed Link: 34417462
Variant Present in the following documents:
  • 41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.

Frontiers In Genetics
Minchiotti, Lorenzo L; Caridi, Gianluca G; Campagnoli, Monica M; Lugani, Francesca F; Galliano, Monica M; Kragh-Hansen, Ulrich U
Publication Date: 2019

Variant appearance in text: GC: 1098dup
PubMed Link: 31057599
Variant Present in the following documents:
  • fgene-10-00336.pdf
View BVdb publication page