ALK c.1155-9139G>A

Variant ID: 2-29615864-C-T

NM_004304.4(ALK):c.1155-9139G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.

Nature Communications
Xue, Yali Y; Mezzavilla, Massimo M; Haber, Marc M; McCarthy, Shane S; Chen, Yuan Y; Narasimhan, Vagheesh V; Gilly, Arthur A; Ayub, Qasim Q; Colonna, Vincenza V; Southam, Lorraine L; Finan, Christopher C; Massaia, Andrea A; Chheda, Himanshu H; Palta, Priit P; Ritchie, Graham G; Asimit, Jennifer J; Dedoussis, George G; Gasparini, Paolo P; Palotie, Aarno A; Ripatti, Samuli S; Soranzo, Nicole N; Toniolo, Daniela D; Wilson, James F JF; Durbin, Richard R; Tyler-Smith, Chris C; Zeggini, Eleftheria E
Publication Date: 2017-06-23

Variant appearance in text: rs13391086
PubMed Link: 28643794
Variant Present in the following documents:
  • ncomms15927-s1.pdf
View BVdb publication page