DNAH11 c.5359T>C ;(p.L1787=)

Variant ID: 7-21721194-T-C

NM_001277115.1(DNAH11):c.5359T>C;(p.L1787=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic variants in African-American and Hispanic patients with breast cancer.

Oncology Letters
Dutta, Pranabananda P; Keung, Man Y MY; Wu, Yanyuan Y; Vadgama, Jaydutt V JV
Publication Date: 2023-02

Variant appearance in text: DNAH11: 5359T>C; L1787L
PubMed Link: 36644153
Variant Present in the following documents:
  • Supplementary_Data5.xlsx, sheet 1
View BVdb publication page



Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways.

Human Genetics
Hagen, Erin M EM; Sicko, Robert J RJ; Kay, Denise M DM; Rigler, Shannon L SL; Dimopoulos, Aggeliki A; Ahmad, Shabbir S; Doleman, Margaret H MH; Fan, Ruzong R; Romitti, Paul A PA; Browne, Marilyn L ML; Caggana, Michele M; Brody, Lawrence C LC; Shaw, Gary M GM; Jelliffe-Pawlowski, Laura L LL; Mills, James L JL
Publication Date: 2016-12

Variant appearance in text: DNAH11: L1787L; rs75932225
PubMed Link: 27637763
Variant Present in the following documents:
  • Main text
View BVdb publication page