NOTCH1 c.1397C>G ;(p.T466S)

Variant ID: 9-139412248-G-C

NM_017617.3(NOTCH1):c.1397C>G;(p.T466S)

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 modifier in the 129S2/SvPasCrl genome is responsible for the viability of Notch1[12f/12f] mice.

Bmc Developmental Biology
Varshney, Shweta S; Wei, Hua-Xing HX; Batista, Frank F; Nauman, Mohd M; Sundaram, Subha S; Siminovitch, Katherine K; Tanwar, Ankit A; Stanley, Pamela P
Publication Date: 2019-10-07

Variant appearance in text: NOTCH1: Thr466Ser
PubMed Link: 31590629
Variant Present in the following documents:
  • Main text
  • 12861_2019_Article_199.pdf
View BVdb publication page