NOTCH1 c.2368A>G ;(p.T790A)

Variant ID: 9-139407572-T-C

NM_017617.3(NOTCH1):c.2368A>G;(p.T790A)

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:

Genetics of Congenital Heart Defects: The NKX2-5 Gene, a Key Player.

Genes
Chung, Ill-Min IM; Rajakumar, Govindasamy G
Publication Date: 2016-01-23

Variant appearance in text: NOTCH1: T790A
PubMed Link: 26805889
Variant Present in the following documents:
  • Main text
  • genes-07-00006.pdf
View BVdb publication page