PARP1 c.412_414delinsTGA ;(p.R138*)

Variant ID: 1-226578314-GCG-TCA

NM_001618.3(PARP1):c.412_414delinsTGA;(p.R138*)

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:

Unique roles of rare variants in the genetics of complex diseases in humans.

Journal Of Human Genetics
Momozawa, Yukihide Y; Mizukami, Keijiro K
Publication Date: 2021-01

Variant appearance in text: PARP: Arg138Ter
PubMed Link: 32948841
Variant Present in the following documents:
  • Main text
View BVdb publication page