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PC c.3008C>T ;(p.T1003M)
Variant ID: 11-66617221-G-A
NM_001040716.1(
PC
):c.3008C>T;(p.T1003M)
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:
Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.
Bmc Gastroenterology
Li, Mingming M; Ma, Jing J; Wang, Wenlong W; Yang, Xu X; Luo, Kaizhong K
Publication Date: 2021-09-01
Variant appearance in text: PC: 3008C>T
PubMed Link:
34470610
Variant Present in the following documents:
12876_2021_Article_1911.pdf
View BVdb publication page
Circulating tumor DNA predicts response in Chinese patients with relapsed or refractory classical hodgkin lymphoma treated with sintilimab.
Ebiomedicine
Shi, Yuankai Y; Su, Hang H; Song, Yongping Y; Jiang, Wenqi W; Sun, Xiuhua X; Qian, Wenbin W; Zhang, Wei W; Gao, Yuhuan Y; Jin, Zhengming Z; Zhou, Jianfeng J; Jin, Chuan C; Zou, Liqun L; Qiu, Lugui L; Li, Wei W; Yang, Jianmin J; Hou, Ming M; Xiong, Yan Y; Zhou, Hui H; Du, Xinhua X; Wang, Xiong X; Peng, Bo B
Publication Date: 2020-04
Variant appearance in text: PC: 3008C>T; T1003M; rs145046106
PubMed Link:
32304999
Variant Present in the following documents:
mmc1.xlsx, sheet 4
View BVdb publication page