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RET c.329G>T ;(p.S110I)
Variant ID: 10-43596162-G-T
NM_020975.4(
RET
):c.329G>T;(p.S110I)
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:
Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.
European Journal Of Human Genetics : Ejhg
McGuigan, Anthony A; Whitworth, James J; Andreou, Avgi A; Hearn, Timothy T; , ; Tischkowitz, Marc M; Maher, Eamonn R ER
Publication Date: 2022-03
Variant appearance in text: RET: 329G>T
PubMed Link:
34983940
Variant Present in the following documents:
41431_2021_1013_MOESM1_ESM.pdf
View BVdb publication page
Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia.
Journal Of Cellular And Molecular Medicine
Wu, Nan N; Zhang, Zhen Z; Zhou, Xi X; Zhao, Hengqiang H; Ming, Yue Y; Wu, Xue X; Zhang, Xian X; Yang, Xin-Zhuang XZ; Zhou, Meng M; Bao, Hua H; Chen, Weisheng W; Wu, Yong Y; Liu, Sen S; Wang, Huizi H; Niu, Yuchen Y; Li, Yalun Y; Zheng, Yu Y; Shao, Yang Y; Gao, Na N; Yang, Ying Y; Liu, Ying Y; Li, Wenli W; Liu, Jia J; Zhang, Na N; Yang, Xu X; Xu, Yuan Y; Li, Mei M; Sun, Yingli Y; Su, Jianzhong J; Zhang, Jianguo J; Xia, Weibo W; Qiu, Guixing G; Liu, Yong Y; Liu, Jiaqi J; Wu, Zhihong Z
Publication Date: 2020-05
Variant appearance in text: RET: 329G>T
PubMed Link:
32277576
Variant Present in the following documents:
JCMM-24-4931-s010.xlsx, sheet 1
View BVdb publication page
Discoveries beyond BRCA1/2: Multigene testing in an Asian multi-ethnic cohort suspected of hereditary breast cancer syndrome in the real world.
Plos One
Ow, Samuel Guan Wei SGW; Ong, Pei Yi PY; Lee, Soo-Chin SC
Publication Date: 2019
Variant appearance in text: RET: 329G>T
PubMed Link:
30875412
Variant Present in the following documents:
View BVdb publication page