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TG c.1958dup ;(p.G654Wfs*10)
Variant ID: 8-133899573-A-AG
NM_003235.4(
TG
):c.1958dup;(p.G654Wfs*10)
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:
The global carrier frequency and genetic prevalence of Upshaw-Schulman syndrome.
Bmc Genomic Data
Zhao, Ting T; Fan, Shanghua S; Sun, Liu L
Publication Date: 2021-11-17
Variant appearance in text: TG: 1957dup
PubMed Link:
34789164
Variant Present in the following documents:
12863_2021_1010_MOESM9_ESM.xlsx, sheet 1
View BVdb publication page
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: TG: 1957dupG
PubMed Link:
34417462
Variant Present in the following documents:
41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page