Home
Toolbox
Resource
Workflow
Tutorials
Citations
Downloads
Mutation Al-Predictor Flow
Gene-to-Mutation Flow
News & Insights
Genetic Encyclopedia
Frontiers
Industry Insights
Case Studies
About Us
About the Site
Contact Us
Private Policy
User Agreement
COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
Log In
|
Sign Up
中文
Create a favorites folder
Cancel
Confirm
Add To Favorites
Select a favorites
Description
New favorites >>
Cancel
Confirm
Favorite
Mutation Direct
Effortless mutation search and display tool
Search
Search criteria:
基因:
NOBOX
& 疾病:
POF1
, 共1条
Search
Reset
ClinVar
基因
碱基改变
氨基酸改变
转录本ID
突变类型
临床意义
疾病数量
文献数量
167875
NOBOX
c.349C>T
p.Arg117Trp (p.R117W)
NM_001080413.3
M
SNV
致病突变
2
+
5
1 Results, 20 per Page
1
微信
信息比对
科研助手
使用教程
回到顶部