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TG c.780dup ;(p.I261Hfs*13)
Variant ID: 8-133894746-A-AC
NM_003235.4(
TG
):c.780dup;(p.I261Hfs*13)
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:
BRCA1/BRCA2 mutation spectrum analysis in South Asia: a systematic review.
The Journal Of International Medical Research
Kharel, Sanjeev S; Shrestha, Suraj S; Yadav, Siddhartha S; Shakya, Prafulla P; Baidya, Sujita S; Hirachan, Suzita S
Publication Date: 2022-01
Variant appearance in text: TG: 779dup
PubMed Link:
35000471
Variant Present in the following documents:
sj-pdf-3-imr-10.1177_03000605211070757.pdf
View BVdb publication page
BRCA1/BRCA2 mutation spectrum analysis in South Asia: a systematic review.
The Journal Of International Medical Research
Kharel, Sanjeev S; Shrestha, Suraj S; Yadav, Siddhartha S; Shakya, Prafulla P; Baidya, Sujita S; Hirachan, Suzita S
Publication Date: 2022-01
Variant appearance in text: TG: 779dup
PubMed Link:
35000471
Variant Present in the following documents:
sj-pdf-3-imr-10.1177_03000605211070757.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: 780dupC
PubMed Link:
34417462
Variant Present in the following documents:
41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page