Bibliome.ai browser hg19
Search
About
Stats
FAQ
KIT c.2465_2466delinsGG ;(p.N822R)
Variant ID: 4-55599339-AT-GG
NM_000222.2(
KIT
):c.2465_2466delinsGG;(p.N822R)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: KIT: N822R
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page
SKP2 high expression, KIT exon 11 deletions, and gastrointestinal bleeding as predictors of poor prognosis in primary gastrointestinal stromal tumors.
Plos One
Lv, Ang A; Li, Zhongwu Z; Tian, Xiuyun X; Guan, Xiaoya X; Zhao, Min M; Dong, Bin B; Hao, Chunyi C
Publication Date: 2013
Variant appearance in text: KIT: N822R
PubMed Link:
23690967
Variant Present in the following documents:
Main text
pone.0062951.pdf
View BVdb publication page