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SHC4 c.657-9318A>G
Variant ID: 15-49192326-T-C
NM_203349.3(
SHC4
):c.657-9318A>G
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:
Papillary renal cell carcinoma: a clinicopathological and whole-genome exon sequencing study.
International Journal Of Clinical And Experimental Pathology
Liu, Kunpeng K; Ren, Yuan Y; Pang, Lijuan L; Qi, Yan Y; Jia, Wei W; Tao, Lin L; Hu, Zhengyan Z; Zhao, Jin J; Zhang, Haijun H; Li, Li L; Yue, Haifeng H; Han, Juan J; Liang, Weihua W; Hu, Jianming J; Zou, Hong H; Yuan, Xianglin X; Li, Feng F
Publication Date: 2015
Variant appearance in text: rs4775785
PubMed Link:
26339402
Variant Present in the following documents:
Main text
View BVdb publication page