EGR1 c.1059_1061del ;(p.D353del)

Variant ID: 5-137803193-CCGA-C

NM_001964.2(EGR1):c.1059_1061del;(p.D353del)

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:

Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma.

Human Mutation
Cardoso, Luís L; Stevenson, Mark M; Thakker, Rajesh V RV
Publication Date: 2017-12

Variant appearance in text: 225: 1058_1060del
PubMed Link: 28881068
Variant Present in the following documents:
  • Main text
  • HUMU-38-1621.pdf
View BVdb publication page