NOC2L c.475_477delinsAAC ;(p.Q159N)

Variant ID: 1-892283-CTG-GTT

NM_015658.3(NOC2L):c.475_477delinsAAC;(p.Q159N)

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:

Mutagenesis of mNeptune Red-Shifts Emission Spectrum to 681-685 nm.

Plos One
Li, ZhaoYang Z; Zhang, ZhiPing Z; Bi, LiJun L; Cui, ZongQiang Z; Deng, JiaoYu J; Wang, DianBing D; Zhang, Xian-En XE
Publication Date: 2016

Variant appearance in text: NIR: Q159N
PubMed Link: 27119418
Variant Present in the following documents:
  • Main text
  • pone.0148749.pdf
View BVdb publication page