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FGD6 c.112A>G ;(p.I38V)
Variant ID: 12-95604948-T-C
NM_018351.3(
FGD6
):c.112A>G;(p.I38V)
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:
Molecular convergence and transgenic evidence suggest a single origin of laryngeal echolocation in bats.
Iscience
Liu, Zhen Z; Chen, Peng P; Xu, Dong-Ming DM; Qi, Fei-Yan FY; Guo, Yuan-Ting YT; Liu, Qi Q; Bai, Jing J; Zhou, Xin X; Shi, Peng P
Publication Date: 2022-04-15
Variant appearance in text: FGD6: I38V
PubMed Link:
35391832
Variant Present in the following documents:
mmc8.xlsx, sheet 1
View BVdb publication page
The landscape of driver mutations in cutaneous squamous cell carcinoma.
Npj Genomic Medicine
Chang, Darwin D; Shain, A Hunter AH
Publication Date: 2021-07-16
Variant appearance in text: FGD6: I38V
PubMed Link:
34272401
Variant Present in the following documents:
41525_2021_226_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page