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DNAH11 c.9192A>T ;(p.R3064S)
Variant ID: 7-21813473-A-T
NM_001277115.1(
DNAH11
):c.9192A>T;(p.R3064S)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
The genomic and epigenomic evolutionary history of papillary renal cell carcinomas.
Nature Communications
Zhu, Bin B; Poeta, Maria Luana ML; Costantini, Manuela M; Zhang, Tongwu T; Shi, Jianxin J; Sentinelli, Steno S; Zhao, Wei W; Pompeo, Vincenzo V; Cardelli, Maurizio M; Alexandrov, Boian S BS; Otlu, Burcak B; Hua, Xing X; Jones, Kristine K; Brodie, Seth S; Dabrowska, Malgorzata Ewa ME; Toro, Jorge R JR; Yeager, Meredith M; Wang, Mingyi M; Hicks, Belynda B; Alexandrov, Ludmil B LB; Brown, Kevin M KM; Wedge, David C DC; Chanock, Stephen S; Fazio, Vito Michele VM; Gallucci, Michele M; Landi, Maria Teresa MT
Publication Date: 2020-06-18
Variant appearance in text: DNAH11: R3064S
PubMed Link:
32555180
Variant Present in the following documents:
41467_2020_16546_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page