SI c.1278G>A ;(p.L426=)

Variant ID: 3-164776956-C-T

NM_001041.3(SI):c.1278G>A;(p.L426=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


An adaptive method of defining negative mutation status for multi-sample comparison using next-generation sequencing.

Bmc Medical Genomics
Hutson, Nicholas N; Zhan, Fenglin F; Graham, James J; Murakami, Mitsuko M; Zhang, Han H; Ganaparti, Sujana S; Hu, Qiang Q; Yan, Li L; Ma, Changxing C; Liu, Song S; Xie, Jun J; Wei, Lei L
Publication Date: 2021-12-02

Variant appearance in text: SI: L426L
PubMed Link: 34856988
Variant Present in the following documents:
  • 12920_2021_880_MOESM1_ESM.xls, sheet 1
View BVdb publication page



An adaptive method of defining negative mutation status for multi-sample comparison using next-generation sequencing.

Bmc Medical Genomics
Hutson, Nicholas N; Zhan, Fenglin F; Graham, James J; Murakami, Mitsuko M; Zhang, Han H; Ganaparti, Sujana S; Hu, Qiang Q; Yan, Li L; Ma, Changxing C; Liu, Song S; Xie, Jun J; Wei, Lei L
Publication Date: 2021-12-02

Variant appearance in text: SI: L426L
PubMed Link: 34856988
Variant Present in the following documents:
  • 12920_2021_880_MOESM1_ESM.xls, sheet 1
View BVdb publication page



A pan-cancer analysis of synonymous mutations.

Nature Communications
Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S
Publication Date: 2019-06-12

Variant appearance in text: SI: 1278G>A
PubMed Link: 31189880
Variant Present in the following documents:
  • 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page