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RHOD c.602_603delinsAT ;(p.R201H)
Variant ID: 11-66839042-GG-AT
NM_014578.3(
RHOD
):c.602_603delinsAT;(p.R201H)
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 prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
Ebiomedicine
Wang, Tao T; Zhao, Tingting T; Liu, Liqiu L; Teng, Huajing H; Fan, Tianda T; Li, Yi Y; Wang, Yan Y; Li, Jinchen J; Xia, Kun K; Sun, Zhongsheng Z
Publication Date: 2022-07
Variant appearance in text: Rho: R201H
PubMed Link:
35665681
Variant Present in the following documents:
mmc24.xlsx, sheet 1
View BVdb publication page
Enrichment of short mutant cell-free DNA fragments enhanced detection of pancreatic cancer.
Ebiomedicine
Liu, Xiaoyu X; Liu, Lingxiao L; Ji, Yuan Y; Li, Changyu C; Wei, Tao T; Yang, Xuerong X; Zhang, Yuefang Y; Cai, Xuyu X; Gao, Yangbin Y; Xu, Weihong W; Rao, Shengxiang S; Jin, Dayong D; Lou, Wenhui W; Qiu, Zilong Z; Wang, Xiaolin X
Publication Date: 2019-03
Variant appearance in text: Rho: R201H
PubMed Link:
30857943
Variant Present in the following documents:
mmc3.xlsx, sheet 2
View BVdb publication page