Bibliome.ai browser hg19
Search
About
Stats
FAQ
NOTCH1 c.1396A>T ;(p.T466S)
Variant ID: 9-139412249-T-A
NM_017617.3(
NOTCH1
):c.1396A>T;(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