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KIT c.229A>C ;(p.N77H)
Variant ID: 4-55561839-A-C
NM_000222.2(
KIT
):c.229A>C;(p.N77H)
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:
Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.
International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017
Variant appearance in text: KIT: 229A>C; Asn77His
PubMed Link:
31966388
Variant Present in the following documents:
Main text
View BVdb publication page