NRAS c.198C>G ;(p.A66=)

Variant ID: 1-115256513-G-C

NM_002524.4(NRAS):c.198C>G;(p.A66=)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Formalin fixation increases deamination mutation signature but should not lead to false positive mutations in clinical practice.

Plos One
Prentice, Leah M LM; Miller, Ruth R RR; Knaggs, Jeff J; Mazloomian, Alborz A; Aguirre Hernandez, Rosalia R; Franchini, Patrick P; Parsa, Kourosh K; Tessier-Cloutier, Basile B; Lapuk, Anna A; Huntsman, David D; Schaeffer, David F DF; Sheffield, Brandon S BS
Publication Date: 2018

Variant appearance in text: NRAS: A66A
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 3
  • pone.0196434.s001.xlsx, sheet 2
View BVdb publication page



Selective identification of somatic mutations in pancreatic cancer cells through a combination of next-generation sequencing of plasma DNA using molecular barcodes and a bioinformatic variant filter.

Plos One
Kukita, Yoji Y; Ohkawa, Kazuyoshi K; Takada, Ryoji R; Uehara, Hiroyuki H; Katayama, Kazuhiro K; Kato, Kikuya K
Publication Date: 2018

Variant appearance in text: NRAS: A66A
PubMed Link: 29451897
Variant Present in the following documents:
  • pone.0192611.s007.xlsx, sheet 1
View BVdb publication page



NRAS and BRAF mutations in melanoma-associated nevi and uninvolved nevi.

Plos One
Tschandl, Philipp P; Berghoff, Anna Sophie AS; Preusser, Matthias M; Burgstaller-Muehlbacher, Sebastian S; Pehamberger, Hubert H; Okamoto, Ichiro I; Kittler, Harald H
Publication Date: 2013

Variant appearance in text: NRAS: A66A
PubMed Link: 23861977
Variant Present in the following documents:
  • Main text
  • pone.0069639.pdf
View BVdb publication page