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VEGFA c.19G>C ;(p.D7H)
Variant ID: 6-43738462-G-C
NM_003376.5(
VEGFA
):c.19G>C;(p.D7H)
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:
Genetic predisposition to necrotizing enterocolitis in premature infants: Current knowledge, challenges, and future directions.
Seminars In Fetal & Neonatal Medicine
Cuna, Alain A; George, Lovya L; Sampath, Venkatesh V
Publication Date: 2018-12
Variant appearance in text: VEGF: D7H
PubMed Link:
30292709
Variant Present in the following documents:
Main text
View BVdb publication page