Bibliome.ai browser hg19
Search
About
Stats
FAQ
FRK c.109T>G ;(p.S37A)
Variant ID: 6-116381366-A-C
NM_002031.2(
FRK
):c.109T>G;(p.S37A)
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:
An autosomal locus that controls chromosome-wide replication timing and mono-allelic expression.
Human Molecular Genetics
Stoffregen, Eric P EP; Donley, Nathan N; Stauffer, Daniel D; Smith, Leslie L; Thayer, Mathew J MJ
Publication Date: 2011-06-15
Variant appearance in text: FRK: S37a
PubMed Link:
21459774
Variant Present in the following documents:
Main text
View BVdb publication page