PON3 c.971G>C ;(p.G324A)

Variant ID: 7-94989379-C-G

NM_000940.2(PON3):c.971G>C;(p.G324A)

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:

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: rs139856535
PubMed Link: 29458409
Variant Present in the following documents:
  • Main text
  • 12993_2018_Article_135.pdf
View BVdb publication page