Bibliome.ai browser hg19
Search
About
Stats
FAQ
KIT c.228G>T ;(p.E76D)
Variant ID: 4-55561838-G-T
NM_000222.2(
KIT
):c.228G>T;(p.E76D)
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:
Towards standardization of next-generation sequencing of FFPE samples for clinical oncology: intrinsic obstacles and possible solutions.
Journal Of Translational Medicine
Ivanov, Maxim M; Laktionov, Konstantin K; Breder, Valery V; Chernenko, Polina P; Novikova, Ekaterina E; Telysheva, Ekaterina E; Musienko, Sergey S; Baranova, Ancha A; Mileyko, Vladislav V
Publication Date: 2017-01-31
Variant appearance in text: KIT: Glu76Asp
PubMed Link:
28137276
Variant Present in the following documents:
Main text
12967_2017_Article_1125.pdf
View BVdb publication page