ETF1 c.1231+84T>A

Variant ID: 5-137844274-A-T

NM_004730.3(ETF1):c.1231+84T>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2242599
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page