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DNAH11 c.3266A>T ;(p.Y1089F)
Variant ID: 7-21640638-A-T
NM_001277115.1(
DNAH11
):c.3266A>T;(p.Y1089F)
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:
Currently favored sampling practices for tumor sequencing can produce optimal results in the clinical setting.
Scientific Reports
Pongor, Lőrinc S LS; Munkácsy, Gyöngyi G; Vereczkey, Ildikó I; Pete, Imre I; Győrffy, Balázs B
Publication Date: 2020-09-01
Variant appearance in text: DNAH11: 3266A>T; Tyr1089Phe
PubMed Link:
32873813
Variant Present in the following documents:
41598_2020_71382_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page