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BRCA2 c.8632+695C>T
Variant ID: 13-32945932-C-T
NM_000059.3(
BRCA2
):c.8632+695C>T
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.
Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22
Variant appearance in text: BRCA2: 8632+695C>T; rs573014
PubMed Link:
31640808
Variant Present in the following documents:
13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
A Chinese family affected by lynch syndrome caused by MLH1 mutation.
Bmc Medical Genetics
Jia, Shuqin S; Zhang, Meng M; Sun, Yu Y; Yan, Hai H; Zhao, Fangping F; Li, Ziyu Z; Ji, Jiafu J
Publication Date: 2018-06-22
Variant appearance in text: rs573014
PubMed Link:
29929473
Variant Present in the following documents:
12881_2018_605_MOESM2_ESM.xlsx, sheet 2
12881_2018_605_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.
Bmc Genetics
Chang, Hsueh-Wei HW; Chuang, Li-Yeh LY; Chang, Yan-Jhu YJ; Cheng, Yu-Huei YH; Hung, Yu-Chen YC; Chen, Hsiang-Chi HC; Yang, Cheng-Hong CH
Publication Date: 2009-06-06
Variant appearance in text: rs573014
PubMed Link:
19500380
Variant Present in the following documents:
Main text
1471-2156-10-26.pdf
View BVdb publication page