NF1 c.1413_1440del ;(p.K471Nfs*18)

Variant ID: 17-29541484-GAAAAAGTAACAAGCCTTAAATTTAAAGA-G

NM_001042492.2(NF1):c.1413_1440del;(p.K471Nfs*18)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.

The Journal Of Clinical Endocrinology And Metabolism
Welander, Jenny J; Andreasson, Adam A; Juhlin, C Christofer CC; Wiseman, Roger W RW; Bäckdahl, Martin M; Höög, Anders A; Larsson, Catharina C; Gimm, Oliver O; Söderkvist, Peter P
Publication Date: 2014-07

Variant appearance in text: NF1: 1413_1440del
PubMed Link: 24694336
Variant Present in the following documents:
  • Main text
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