SI c.550_552delinsGAC ;(p.T184D)

Variant ID: 3-164785211-TGT-GTC

NM_001041.3(SI):c.550_552delinsGAC;(p.T184D)

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:

Premature Cdk1/Cdc5/Mus81 pathway activation induces aberrant replication and deleterious crossover.

The Embo Journal
Szakal, Barnabas B; Branzei, Dana D
Publication Date: 2013-04-17

Variant appearance in text: SI: T184D
PubMed Link: 23531881
Variant Present in the following documents:
  • Main text
  • emboj201367a.pdf
View BVdb publication page