NOP58 c.1402+444C>T

Variant ID: 2-203165534-C-T

NM_015934.3(NOP58):c.1402+444C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of microdeletions in candidate genes for cleft lip and/or palate.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Shi, Min M; Mostowska, Adrianna A; Jugessur, Astanand A; Johnson, Marla K MK; Mansilla, Maria Adela MA; Christensen, Kaare K; Lie, Rolv T RT; Wilcox, Allen J AJ; Murray, Jeffrey C JC
Publication Date: 2009-01

Variant appearance in text: rs6753156
PubMed Link: 19137569
Variant Present in the following documents:
  • Main text
View BVdb publication page