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F2 c.438C>T ;(p.T146=)
Variant ID: 11-46744947-C-T
NM_000506.3(
F2
):c.438C>T;(p.T146=)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Goal discrimination in hippocampal nonplace cells when place information is ambiguous.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Zhang, Lu L; Prince, Stephanie M SM; Paulson, Abigail L AL; Singer, Annabelle C AC
Publication Date: 2022-03-15
Variant appearance in text: F2: t146=
PubMed Link:
35254897
Variant Present in the following documents:
pnas.2107337119.sapp.pdf
View BVdb publication page
Detecting rare triple heteroplasmic substitutions in the mitochondrial DNA control region: a potential concern for forensic DNA studies.
Cell Journal
Morovvati, Saeid S; Morovvati, Ziba Z; Ranjbar, Reza R
Publication Date: 2011
Variant appearance in text: F2: T146T
PubMed Link:
23508063
Variant Present in the following documents:
Main text
Cell-J-13-103.pdf
View BVdb publication page