AVP c.338A>G ;(p.E113G)

Variant ID: 20-3063433-T-C

NM_000490.4(AVP):c.338A>G;(p.E113G)

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:

Effective mismatch repair depends on timely control of PCNA retention on DNA by the Elg1 complex.

Nucleic Acids Research
Paul Solomon Devakumar, Lovely Jael LJ; Gaubitz, Christl C; Lundblad, Victoria V; Kelch, Brian A BA; Kubota, Takashi T
Publication Date: 2019-07-26

Variant appearance in text: ADH: E113G
PubMed Link: 31114918
Variant Present in the following documents:
  • Main text
  • gkz441.pdf
View BVdb publication page