EEFSEC c.1601-4516G>A

Variant ID: 3-128122396-G-A

NM_021937.3(EEFSEC):c.1601-4516G>A

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites.

Human Mutation
Bu, Huajie H; Narisu, Narisu N; Schlick, Bettina B; Rainer, Johannes J; Manke, Thomas T; Schäfer, Georg G; Pasqualini, Lorenza L; Chines, Peter P; Schweiger, Michal R MR; Fuchsberger, Christian C; Klocker, Helmut H
Publication Date: 2016-01

Variant appearance in text: rs2659685
PubMed Link: 26411452
Variant Present in the following documents:
  • HUMU-37-52-s001.pdf
View BVdb publication page