FLT4 c.3344A>G ;(p.Y1115C)

Variant ID: 5-180040098-T-C

NM_182925.4(FLT4):c.3344A>G;(p.Y1115C)

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:

A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects.

European Journal Of Medical Research
Tabib, Avisa A; Talebi, Taravat T; Ghasemi, Serwa S; Pourirahim, Maryam M; Naderi, Niloofar N; Maleki, Majid M; Kalayinia, Samira S
Publication Date: 2022-12-10

Variant appearance in text: FLT4: Y1115C
PubMed Link: 36496429
Variant Present in the following documents:
  • Main text
  • 40001_2022_Article_920.pdf
View BVdb publication page