TSPAN2 c.211_213delinsCAA ;(p.A71Q)

Variant ID: 1-115604813-GGC-TTG

NM_005725.4(TSPAN2):c.211_213delinsCAA;(p.A71Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Systematic discovery of complex insertions and deletions in human cancers.

Nature Medicine
Ye, Kai K; Wang, Jiayin J; Jayasinghe, Reyka R; Lameijer, Eric-Wubbo EW; McMichael, Joshua F JF; Ning, Jie J; McLellan, Michael D MD; Xie, Mingchao M; Cao, Song S; Yellapantula, Venkata V; Huang, Kuan-lin KL; Scott, Adam A; Foltz, Steven S; Niu, Beifang B; Johnson, Kimberly J KJ; Moed, Matthijs M; Slagboom, P Eline PE; Chen, Feng F; Wendl, Michael C MC; Ding, Li L
Publication Date: 2016-01

Variant appearance in text: TSPAN2: A71Q
PubMed Link: 26657142
Variant Present in the following documents:
  • NIHMS735489-supplement-5.xlsx, sheet 1
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