Bibliome.ai browser hg19
Search
About
Stats
FAQ
WARS2 c.452A>G ;(p.H151R)
Variant ID: 1-119584950-T-C
NM_015836.3(
WARS2
):c.452A>G;(p.H151R)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.
Nature Communications
Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B
Publication Date: 2020-04-09
Variant appearance in text: WARS2: H151R
PubMed Link:
32273506
Variant Present in the following documents:
41467_2020_15456_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion.
Behavioral And Brain Functions : Bbf
Varga, Noémi Ágnes NÁ; Pentelényi, Klára K; Balicza, Péter P; Gézsi, András A; Reményi, Viktória V; Hársfalvi, Vivien V; Bencsik, Renáta R; Illés, Anett A; Prekop, Csilla C; Molnár, Mária Judit MJ
Publication Date: 2018-02-20
Variant appearance in text: WARS2: H151R; rs150022801
PubMed Link:
29458409
Variant Present in the following documents:
Main text
12993_2018_Article_135.pdf
View BVdb publication page