HERC2 c.14479A>G ;(p.T4827A)

Variant ID: 15-28356935-T-C

NM_004667.5(HERC2):c.14479A>G;(p.T4827A)

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:

DNA damage-inducible SUMOylation of HERC2 promotes RNF8 binding via a novel SUMO-binding Zinc finger.

The Journal Of Cell Biology
Danielsen, Jannie Rendtlew JR; Povlsen, Lou Klitgaard LK; Villumsen, Bine Hare BH; Streicher, Werner W; Nilsson, Jakob J; Wikström, Mats M; Bekker-Jensen, Simon S; Mailand, Niels N
Publication Date: 2012-04-16

Variant appearance in text: HERC2: T4827A
PubMed Link: 22508508
Variant Present in the following documents:
  • Main text
  • JCB_201106152.pdf
View BVdb publication page