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TTN c.30587T>C ;(p.V10196A)
Variant ID: 2-179566266-A-G
NM_001267550.1(
TTN
):c.30587T>C;(p.V10196A)
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:
Integrative analysis reveals clinically relevant molecular fingerprints in pancreatic cancer.
Molecular Therapy. Nucleic Acids
Song, Libin L; Qi, Simin S; Hu, Wei W; Fang, Zhixiao Z; Yu, Dehua D; Liu, Teng T; Wu, Jingni J; Wu, Yangjun Y; Wu, Aiwei A; Feng, Lanyun L; Xie, Jing J; Zhang, Bo B; He, Wenguang W; Ning, Zhouyu Z; Liu, Luming L; Qin, Jiang-Jiang JJ; Li, Shengli S
Publication Date: 2021-12-03
Variant appearance in text: TTN: 30587T>C; V10196A
PubMed Link:
34513290
Variant Present in the following documents:
mmc3.xlsx, sheet 1
View BVdb publication page
The genetic landscape of benign thyroid nodules revealed by whole exome and transcriptome sequencing.
Nature Communications
Ye, Lei L; Zhou, Xiaoyi X; Huang, Fengjiao F; Wang, Weixi W; Qi, Yicheng Y; Xu, Heng H; Yang, Shu S; Shen, Liyun L; Fei, Xiaochun X; Xie, Jing J; Cao, Min M; Zhou, Yulin Y; Zhu, Wei W; Wang, Shu S; Ning, Guang G; Wang, Weiqing W
Publication Date: 2017-06-05
Variant appearance in text: TTN: V10196A
PubMed Link:
28580939
Variant Present in the following documents:
ncomms15533-s4.xlsx, sheet 1
View BVdb publication page