F2 c.480C>G ;(p.P160=)

Variant ID: 11-46744989-C-G

NM_000506.3(F2):c.480C>G;(p.P160=)

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:

Unified tests for fine-scale mapping and identifying sparse high-dimensional sequence associations.

Bioinformatics (Oxford, England)
Cao, Shaolong S; Qin, Huaizhen H; Gossmann, Alexej A; Deng, Hong-Wen HW; Wang, Yu-Ping YP
Publication Date: 2016-02-01

Variant appearance in text: rs3136452
PubMed Link: 26458888
Variant Present in the following documents:
  • Main text
View BVdb publication page