ERBB2 c.2724_2725insA ;(p.G909Rfs*25)

Variant ID: 17-37881654-T-TA

NM_004448.2(ERBB2):c.2724_2725insA;(p.G909Rfs*25)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A system for detecting high impact-low frequency mutations in primary tumors and metastases.

Oncogene
Anjanappa, M M; Hao, Y Y; Simpson, E R ER; Bhat-Nakshatri, P P; Nelson, J B JB; Tersey, S A SA; Mirmira, R G RG; Cohen-Gadol, A A AA; Saadatzadeh, M R MR; Li, L L; Fang, F F; Nephew, K P KP; Miller, K D KD; Liu, Y Y; Nakshatri, H H
Publication Date: 2018-01-11

Variant appearance in text: ERBB2: G909fs
PubMed Link: 28892047
Variant Present in the following documents:
  • Main text
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