DNAH11 c.4237_4239delinsTTT ;(p.L1413F)

Variant ID: 7-21657378-CTG-TTT

NM_001277115.1(DNAH11):c.4237_4239delinsTTT;(p.L1413F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Modeling cancer driver events in vitro using barrier bypass-clonal expansion assays and massively parallel sequencing.

Oncogene
Huskova, H H; Ardin, M M; Weninger, A A; Vargova, K K; Barrin, S S; Villar, S S; Olivier, M M; Stopka, T T; Herceg, Z Z; Hollstein, M M; Zavadil, J J; Korenjak, M M
Publication Date: 2017-10-26

Variant appearance in text: Dnahc11: L1413F
PubMed Link: 28692054
Variant Present in the following documents:
  • onc2017215x4.xls, sheet 1
View BVdb publication page