EGF c.213G>T ;(p.V71=)

Variant ID: 4-110862187-G-T

NM_001963.4(EGF):c.213G>T;(p.V71=)

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:

Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study.

Cns Neuroscience & Therapeutics
Chen, Sheng S; Ni, Wang W; Yin, Xin-Zhen XZ; Liu, Han-Qiu HQ; Lu, Cong C; Zheng, Qiao-Juan QJ; Zhao, Gui-Xian GX; Xu, Yong-Feng YF; Wu, Lei L; Zhang, Liang L; Wang, Ning N; Li, Hong-Fu HF; Wu, Zhi-Ying ZY
Publication Date: 2017-09

Variant appearance in text: EGF: 213G>T
PubMed Link: 28710804
Variant Present in the following documents:
  • Main text
View BVdb publication page