EGR1 c.771_775del ;(p.F257Lfs*35)

Variant ID: 5-137802909-TTCCAC-T

NM_001964.2(EGR1):c.771_775del;(p.F257Lfs*35)

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:

Human BRCA pathogenic variants were originated during recent human history.

Life Science Alliance
Li, Jiaheng J; Zhao, Bojin B; Huang, Teng T; Qin, Zixin Z; Wang, San Ming SM
Publication Date: 2022-05

Variant appearance in text: 225: 771_775del
PubMed Link: 35165121
Variant Present in the following documents:
  • LSA-2021-01263.pdf
View BVdb publication page