DNAH11 c.13310G>A ;(p.R4437H)

Variant ID: 7-21940631-G-A

NM_001277115.1(DNAH11):c.13310G>A;(p.R4437H)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Comprehensive omic characterization of breast cancer in Mexican-Hispanic women.

Nature Communications
Romero-Cordoba, Sandra L SL; Salido-Guadarrama, Ivan I; Rebollar-Vega, Rosa R; Bautista-Piña, Veronica V; Dominguez-Reyes, Carlos C; Tenorio-Torres, Alberto A; Villegas-Carlos, Felipe F; Fernández-López, Juan C JC; Uribe-Figueroa, Laura L; Alfaro-Ruiz, Luis L; Hidalgo-Miranda, Alfredo A
Publication Date: 2021-04-14

Variant appearance in text: DNAH11: R4437H
PubMed Link: 33854067
Variant Present in the following documents:
  • 41467_2021_22478_MOESM8_ESM.xlsx, sheet 9
View BVdb publication page



NOTCH and DNA repair pathways are more frequently targeted by genomic alterations in inflammatory than in non-inflammatory breast cancers.

Molecular Oncology
Bertucci, François F; Rypens, Charlotte C; Finetti, Pascal P; Guille, Arnaud A; Adélaïde, José J; Monneur, Audrey A; Carbuccia, Nadine N; Garnier, Séverine S; Dirix, Piet P; Gonçalves, Anthony A; Vermeulen, Peter P; Debeb, Bisrat G BG; Wang, Xiaoping X; Dirix, Luc L; Ueno, Naoto T NT; Viens, Patrice P; Cristofanilli, Massimo M; Chaffanet, Max M; Birnbaum, Daniel D; Van Laere, Steven S
Publication Date: 2020-03

Variant appearance in text: DNAH11: R4437H
PubMed Link: 31854063
Variant Present in the following documents:
  • MOL2-14-504-s010.xlsx, sheet 1
View BVdb publication page



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: 13310G>A
PubMed Link: 30359267
Variant Present in the following documents:
  • Main text
  • 12920_2018_Article_409.pdf
View BVdb publication page