Bibliome.ai browser hg19
Search
About
Stats
FAQ
KIT c.1513_1514delinsGT ;(p.N505V)
Variant ID: 4-55592189-AA-GT
NM_000222.2(
KIT
):c.1513_1514delinsGT;(p.N505V)
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:
Lack of SF3B1 R625 mutations in cutaneous melanoma.
Diagnostic Pathology
Schilling, Bastian B; Bielefeld, Nicola N; Sucker, Antje A; Hillen, Uwe U; Zimmer, Lisa L; Schadendorf, Dirk D; Zeschnigk, Michael M; Griewank, Klaus G KG
Publication Date: 2013-05-21
Variant appearance in text: KIT: N505V
PubMed Link:
23694694
Variant Present in the following documents:
Main text
1746-1596-8-87.pdf
View BVdb publication page