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TG c.4066del ;(p.C1356Vfs*2)
Variant ID: 8-133923683-GT-G
NM_003235.4(
TG
):c.4066del;(p.C1356Vfs*2)
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:
Prevalence of BRCA1 and BRCA2 pathogenic sequence variants in ovarian cancer patients in the Gulf region: the PREDICT study.
Bmc Cancer
Azribi, Fathi F; Abdou, Ehab E; Dawoud, Emad E; Ashour, Mohamed M; Kamal, Amgad A; Al Sayed, Mohamed M; Burney, Ikram I
Publication Date: 2021-12-20
Variant appearance in text: TG: 4065_4065del
PubMed Link:
34930165
Variant Present in the following documents:
12885_2021_Article_9094.pdf
View BVdb publication page
Prevalence of BRCA1 and BRCA2 pathogenic sequence variants in ovarian cancer patients in the Gulf region: the PREDICT study.
Bmc Cancer
Azribi, Fathi F; Abdou, Ehab E; Dawoud, Emad E; Ashour, Mohamed M; Kamal, Amgad A; Al Sayed, Mohamed M; Burney, Ikram I
Publication Date: 2021-12-20
Variant appearance in text: TG: 4065_4065del
PubMed Link:
34930165
Variant Present in the following documents:
12885_2021_Article_9094.pdf
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: 4065delT
PubMed Link:
34417462
Variant Present in the following documents:
41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page