DNAH11 c.778A>C ;(p.R260=)

Variant ID: 7-21599306-A-C

NM_001277115.1(DNAH11):c.778A>C;(p.R260=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).

Bmc Medical Genomics
Leung, Gordon K C GKC; Mak, Christopher C Y CCY; Fung, Jasmine L F JLF; Wong, Wilfred H S WHS; Tsang, Mandy H Y MHY; Yu, Mullin H C MHC; Pei, Steven L C SLC; Yeung, K S KS; Mok, Gary T K GTK; Lee, C P CP; Hui, Amelia P W APW; Tang, Mary H Y MHY; Chan, Kelvin Y K KYK; Liu, Anthony P Y APY; Yang, Wanling W; Sham, P C PC; Kan, Anita S Y ASY; Chung, Brian H Y BHY
Publication Date: 2018-10-25

Variant appearance in text: DNAH11: 778A>C
PubMed Link: 30359267
Variant Present in the following documents:
  • Main text
  • 12920_2018_Article_409.pdf
View BVdb publication page