DNAH11 c.7220dup ;(p.F2408Ifs*18)

Variant ID: 7-21760427-G-GT

NM_001277115.1(DNAH11):c.7220dup;(p.F2408Ifs*18)

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:

Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.

Esc Heart Failure
Yi, Tong T; Hao, Xiaoyan X; Sun, Hairui H; Zhang, Ye Y; Han, Jiancheng J; Gu, Xiaoyan X; Sun, Lin L; Liu, Xiaowei X; Zhao, Ying Y; Guo, Yong Y; Zhou, Xiaoxue X; He, Yihua Y
Publication Date: 2022-12-07

Variant appearance in text: DNAH11: 7220dupT
PubMed Link: 36478645
Variant Present in the following documents:
  • EHF2-10-917.pdf
View BVdb publication page