SI c.443T>A ;(p.F148Y)

Variant ID: 3-164786550-A-T

NM_001041.3(SI):c.443T>A;(p.F148Y)

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:

TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.

Human Molecular Genetics
Gao, Shan S; Moreno, Myriam M; Eliason, Steven S; Cao, Huojun H; Li, Xiao X; Yu, Wenjie W; Bidlack, Felicitas B FB; Margolis, Henry C HC; Baldini, Antonio A; Amendt, Brad A BA
Publication Date: 2015-04-15

Variant appearance in text: SI: F148Y
PubMed Link: 25556186
Variant Present in the following documents:
  • Main text
View BVdb publication page