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KIT c.2056_2057insA ;(p.R686Qfs*2)
Variant ID: 4-55595566-C-CA
NM_000222.2(
KIT
):c.2056_2057insA;(p.R686Qfs*2)
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:
Dynamic recurrence risk and adjuvant chemotherapy benefit prediction by ctDNA in resected NSCLC.
Nature Communications
Qiu, Bin B; Guo, Wei W; Zhang, Fan F; Lv, Fang F; Ji, Ying Y; Peng, Yue Y; Chen, Xiaoxi X; Bao, Hua H; Xu, Yang Y; Shao, Yang Y; Tan, Fengwei F; Xue, Qi Q; Gao, Shugeng S; He, Jie J
Publication Date: 2021-11-19
Variant appearance in text: KIT: 2056_2057insA; R686Qfs*2
PubMed Link:
34799585
Variant Present in the following documents:
41467_2021_27022_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
Dynamic recurrence risk and adjuvant chemotherapy benefit prediction by ctDNA in resected NSCLC.
Nature Communications
Qiu, Bin B; Guo, Wei W; Zhang, Fan F; Lv, Fang F; Ji, Ying Y; Peng, Yue Y; Chen, Xiaoxi X; Bao, Hua H; Xu, Yang Y; Shao, Yang Y; Tan, Fengwei F; Xue, Qi Q; Gao, Shugeng S; He, Jie J
Publication Date: 2021-11-19
Variant appearance in text: KIT: 2056_2057insA; R686Qfs*2
PubMed Link:
34799585
Variant Present in the following documents:
41467_2021_27022_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page