Bibliome.ai browser hg19
Search
About
Stats
FAQ
TG c.929dup ;(p.S310Rfs*51)
Variant ID: 8-133895097-A-AG
NM_003235.4(
TG
):c.929dup;(p.S310Rfs*51)
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:
Gene-specific machine learning model to predict the pathogenicity of BRCA2 variants.
Frontiers In Genetics
Khandakji, Mohannad N MN; Mifsud, Borbala B
Publication Date: 2022
Variant appearance in text: TG: 929dup
PubMed Link:
36246618
Variant Present in the following documents:
Table1.xlsx, sheet 3
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: 929dupG
PubMed Link:
34417462
Variant Present in the following documents:
41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page