DNAH11 c.8277T>A ;(p.F2759L)

Variant ID: 7-21784178-T-A

NM_001277115.1(DNAH11):c.8277T>A;(p.F2759L)

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:

DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome.

Scientific Reports
Liu, Sida S; Chen, Weicheng W; Zhan, Yongkun Y; Li, Shuolin S; Ma, Xiaojing X; Ma, Duan D; Sheng, Wei W; Huang, Guoying G
Publication Date: 2019-04-30

Variant appearance in text: DNAH11: F2759L
PubMed Link: 31040315
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_43109.pdf
View BVdb publication page