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EGF c.1655A>C ;(p.E552A)
Variant ID: 4-110890206-A-C
NM_001963.4(
EGF
):c.1655A>C;(p.E552A)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Characterization of familial breast cancer in Saudi Arabia.
Bmc Genomics
Merdad, Adnan A; Gari, Mamdooh A MA; Hussein, Shireen S; Al-Khayat, Shadi S; Tashkandi, Hana H; Al-Maghrabi, Jaudah J; Al-Thubaiti, Fatma F; Hussein, Ibtessam R IR; Koumosani, Taha T; Shaer, Nehad N; Chaudhary, Adeel G AG; Abuzenadah, Adel M AM; Al-Qahtani, Mohammed H MH; Dallol, Ashraf A
Publication Date: 2015
Variant appearance in text: EGF: 1655A>C
PubMed Link:
25923920
Variant Present in the following documents:
Main text
1471-2164-16-S1-S3.pdf
View BVdb publication page
Glanzmann thrombasthenia: state of the art and future directions.
Seminars In Thrombosis And Hemostasis
Nurden, Alan T AT; Pillois, Xavier X; Wilcox, David A DA
Publication Date: 2013-09
Variant appearance in text: EGF: Glu552Ala
PubMed Link:
23929305
Variant Present in the following documents:
Main text
View BVdb publication page