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TG c.4829_4830del ;(p.D1610Gfs*18)
Variant ID: 8-133945818-GAC-G
NM_003235.4(
TG
):c.4829_4830del;(p.D1610Gfs*18)
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:
Ethnic-specificity, evolution origin and deleteriousness of Asian BRCA variation revealed by over 7500 BRCA variants derived from Asian population.
International Journal Of Cancer
Qin, Zixin Z; Li, Jiaheng J; Tam, Benjamin B; Sinha, Siddharth S; Zhao, Bojin B; Bhaskaran, Shanmuga Priya SP; Huang, Teng T; Wu, Xiaobing X; Chian, Jia Sheng JS; Guo, Maoni M; Kou, Si Hoi SH; Lei, Huijun H; Zhang, Li L; Wang, Xiaoyu X; Lagniton, Philip Naderev P PNP; Xiao, Fengxia F; Jiang, Xinyang X; Wang, San Ming SM
Publication Date: 2022-11-17
Variant appearance in text: TG: 4829_4830del
PubMed Link:
36385461
Variant Present in the following documents:
IJC-152-1159-s006.xlsx, sheet 3
IJC-152-1159-s002.xlsx, sheet 2
IJC-152-1159-s011.xlsx, sheet 2
View BVdb publication page
Distinct landscapes of deleterious variants in DNA damage repair system in ethnic human populations.
Life Science Alliance
Qin, Zixin Z; Huang, Teng T; Guo, Maoni M; Wang, San Ming SM
Publication Date: 2022-09
Variant appearance in text: TG: 4829_4830del
PubMed Link:
35595529
Variant Present in the following documents:
LSA-2021-01319_TableS5.xlsx, sheet 1
View BVdb publication page