UNG c.686G>A ;(p.R229Q)

Variant ID: 12-109541301-G-A

NM_080911.2(UNG):c.686G>A;(p.R229Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: UNG: R229Q; rs146408261
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Genetic variability in DNA repair proteins in age-related macular degeneration.

International Journal Of Molecular Sciences
Blasiak, Janusz J; Synowiec, Ewelina E; Salminen, Antero A; Kaarniranta, Kai K
Publication Date: 2012-10-18

Variant appearance in text: UNG: R229Q
PubMed Link: 23202958
Variant Present in the following documents:
  • ijms-13-13378.pdf
View BVdb publication page