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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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