NOTCH1 c.1139C>T ;(p.P380L)

Variant ID: 9-139412705-G-A

NM_017617.3(NOTCH1):c.1139C>T;(p.P380L)

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:

Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neoplasms.

Plos One
Kim, Borahm B; Lee, Hyeonah H; Jang, Jieun J; Kim, Soo-Jeong SJ; Lee, Seung-Tae ST; Cheong, June-Won JW; Lyu, Chuhl Joo CJ; Min, Yoo Hong YH; Choi, Jong Rak JR
Publication Date: 2019

Variant appearance in text: NOTCH1: 1139C>T; Pro380Leu
PubMed Link: 30840646
Variant Present in the following documents:
  • pone.0212228.s004.pdf
View BVdb publication page