NRAS c.548G>C ;(p.G183A)

Variant ID: 1-115251178-C-G

NM_002524.4(NRAS):c.548G>C;(p.G183A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.

Nature Communications
Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ
Publication Date: 2017-05-11

Variant appearance in text: rs559507315
PubMed Link: 28492226
Variant Present in the following documents:
  • ncomms15086-s3.xlsx, sheet 1
View BVdb publication page



Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing.

Bioinformatics And Biology Insights
Kan, Takatsugu T; Paun, Bogdan C BC; Mori, Yuriko Y; Sato, Fumiaki F; Jin, Zhe Z; Hamilton, James P JP; Ito, Tetsuo T; Cheng, Yulan Y; David, Stefan S; Olaru, Alexandru V AV; Yang, Jian J; Agarwal, Rachana R; Abraham, John M JM; Meltzer, Stephen J SJ
Publication Date: 2007

Variant appearance in text: NRAS: G183A
PubMed Link: 18389087
Variant Present in the following documents:
  • Main text
  • bbi-2007-001.pdf
View BVdb publication page