ATM c.3295del ;(p.D1099Tfs*10)

Variant ID: 11-108150226-AG-A

NM_000051.3(ATM):c.3295del;(p.D1099Tfs*10)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Human GRIN2B variants in neurodevelopmental disorders.

Journal Of Pharmacological Sciences
Hu, Chun C; Chen, Wenjuan W; Myers, Scott J SJ; Yuan, Hongjie H; Traynelis, Stephen F SF
Publication Date: 2016-10

Variant appearance in text: ATD: 3295del
PubMed Link: 27818011
Variant Present in the following documents:
  • Main text
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