GC c.47C>G ;(p.A16G)

Variant ID: 4-72649689-G-C

NM_000583.3(GC):c.47C>G;(p.A16G)

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Co-crystal structures of the fluorogenic aptamer Beetroot show that close homology may not predict similar RNA architecture.

Nature Communications
Passalacqua, Luiz F M LFM; Starich, Mary R MR; Link, Katie A KA; Wu, Jiahui J; Knutson, Jay R JR; Tjandra, Nico N; Jaffrey, Samie R SR; Ferré-D'Amaré, Adrian R AR
Publication Date: 2023-05-23

Variant appearance in text: GC: A16G
PubMed Link: 37221204
Variant Present in the following documents:
  • 41467_2023_Article_38683.pdf
View BVdb publication page



HaploCoV: unsupervised classification and rapid detection of novel emerging variants of SARS-CoV-2.

Communications Biology
Chiara, Matteo M; Horner, David S DS; Ferrandi, Erika E; Gissi, Carmela C; Pesole, Graziano G
Publication Date: 2023-04-22

Variant appearance in text: GC: 47C>G; A16G
PubMed Link: 37087497
Variant Present in the following documents:
  • 42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Genomic stability at the coding regions of the multidrug transporter gene ABCB1: insights into the development of alternative drug resistance mechanisms in human leukemia cells.

Cancer Drug Resistance (Alhambra, Calif.)
Chen, Kevin G KG; Duran, George E GE; Mogul, Mark J MJ; Wang, Yan C YC; Ross, Kevin L KL; Jaffrézou, Jean-Pierre JP; Huff, Lyn M LM; Johnson, Kory R KR; Fojo, Tito T; Lacayo, Norman J NJ; Sikic, Branimir I BI
Publication Date: 2020

Variant appearance in text: GC: 47C>G
PubMed Link: 34541464
Variant Present in the following documents:
  • cdr-3-959-SupplementaryMaterials.xlsx, sheet 1
View BVdb publication page



K-Ras-Activated Cells Can Develop into Lung Tumors When Runx3-Mediated Tumor Suppressor Pathways Are Abrogated.

Molecules And Cells
Lee, You-Soub YS; Lee, Ja-Yeol JY; Song, Soo-Hyun SH; Kim, Da-Mi DM; Lee, Jung-Won JW; Chi, Xin-Zi XZ; Ito, Yoshiaki Y; Bae, Suk-Chul SC
Publication Date: 2020-10-31

Variant appearance in text: GC: 47C>G; Ala16Gly
PubMed Link: 33115981
Variant Present in the following documents:
  • molce-43-889_Supple.xlsx, sheet 1
View BVdb publication page



Single-stranded binding proteins and helicase enhance the activity of prokaryotic argonautes in vitro.

Plos One
Hunt, Eric A EA; Evans, Thomas C TC; Tanner, Nathan A NA
Publication Date: 2018

Variant appearance in text: GC: A16G
PubMed Link: 30157272
Variant Present in the following documents:
  • pone.0203073.s009.pdf
View BVdb publication page



Comparative analysis of primary versus relapse/refractory DLBCL identifies shifts in mutation spectrum.

Oncotarget
Greenawalt, Danielle M DM; Liang, Winnie S WS; Saif, Sakina S; Johnson, Justin J; Todorov, Petar P; Dulak, Austin A; Enriquez, Daniel D; Halperin, Rebecca R; Ahmed, Ambar A; Saveliev, Vladislav V; Carpten, John J; Craig, David D; Barrett, J Carl JC; Dougherty, Brian B; Zinda, Michael M; Fawell, Stephen S; Dry, Jonathan R JR; Byth, Kate K
Publication Date: 2017-11-21

Variant appearance in text: GC: 47C>G
PubMed Link: 29245897
Variant Present in the following documents:
  • oncotarget-08-99237-s002.xlsx, sheet 1
View BVdb publication page



Diagnostic Performance of the GenoType MTBDRplus and MTBDRsl Assays to Identify Tuberculosis Drug Resistance in Eastern China.

Chinese Medical Journal
Liu, Qiao Q; Li, Guo-Li GL; Chen, Cheng C; Wang, Jian-Ming JM; Martinez, Leonardo L; Lu, Wei W; Zhu, Li-Mei LM
Publication Date: 2017-07-05

Variant appearance in text: GC: A16G
PubMed Link: 28639565
Variant Present in the following documents:
  • CMJ-130-1521.pdf
View BVdb publication page



Whole-Genome Resequencing Identifies the Molecular Genetic Cause for the Absence of a Gy5 Glycinin Protein in Soybean PI 603408.

G3 (Bethesda, Md.)
Gillman, Jason D JD; Kim, Won-Seok WS; Song, Bo B; Oehrle, Nathan W NW; Tawari, Nilesh R NR; Liu, Shanshan S; Krishnan, Hari B HB
Publication Date: 2017-07-05

Variant appearance in text: GC: Ala16Gly
PubMed Link: 28592556
Variant Present in the following documents:
  • 2345FileS1.xlsx, sheet 1
View BVdb publication page



Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness.

Bmc Ear, Nose, And Throat Disorders
Ji, Haiting H; Lu, Jingqiao J; Wang, Jianjun J; Li, Huawei H; Lin, Xi X
Publication Date: 2014

Variant appearance in text: GC: A16G
PubMed Link: 25342930
Variant Present in the following documents:
  • Main text
  • 1472-6815-14-9.pdf
View BVdb publication page