ABCB4 c.1460C>G ;(p.A487G)

Variant ID: 7-87069615-G-C

NM_000443.3(ABCB4):c.1460C>G;(p.A487G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.

Molecular Autism
Codina-Solà, Marta M; Rodríguez-Santiago, Benjamín B; Homs, Aïda A; Santoyo, Javier J; Rigau, Maria M; Aznar-Laín, Gemma G; Del Campo, Miguel M; Gener, Blanca B; Gabau, Elisabeth E; Botella, María Pilar MP; Gutiérrez-Arumí, Armand A; Antiñolo, Guillermo G; Pérez-Jurado, Luis Alberto LA; Cuscó, Ivon I
Publication Date: 2015

Variant appearance in text: ABCB4: A487G
PubMed Link: 25969726
Variant Present in the following documents:
  • 13229_2015_17_MOESM2_ESM.xlsx, sheet 7
View BVdb publication page