TG c.157_159delinsTTT ;(p.A53F)

Variant ID: 8-133880449-GCA-TTT

NM_003235.4(TG):c.157_159delinsTTT;(p.A53F)

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:

Convergence of biomarkers and risk factor trait loci of coronary artery disease at 3p21.31 and HLA region.

Npj Genomic Medicine
Nikpay, Majid M; McPherson, Ruth R
Publication Date: 2021-02-11

Variant appearance in text: TG: A53F
PubMed Link: 33574266
Variant Present in the following documents:
  • Main text
View BVdb publication page