ERBB2 c.205_206delinsTT ;(p.A69F)

Variant ID: 17-37863374-GC-TT

NM_004448.2(ERBB2):c.205_206delinsTT;(p.A69F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: ERBB2: A69F
PubMed Link: 34051734
Variant Present in the following documents:
  • Main text
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