PKD1 c.10720_10721insAGGG ;(p.G3574Efs*54)

Variant ID: 16-2143912-C-CCCCT

NM_001009944.2(PKD1):c.10720_10721insAGGG;(p.G3574Efs*54)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Nephroplex: a kidney-focused NGS panel highlights the challenges of PKD1 sequencing and identifies a founder BBS4 mutation.

Journal Of Nephrology
Zacchia, Miriam M; Blanco, Francesca Del Vecchio FDV; Trepiccione, Francesco F; Blasio, Giancarlo G; Torella, Annalaura A; Melluso, Andrea A; Capolongo, Giovanna G; Pollastro, Rosa Maria RM; Piluso, Giulio G; Di Iorio, Valentina V; Simonelli, Francesca F; Viggiano, Davide D; Perna, Alessandra A; Nigro, Vincenzo V; Capasso, Giovambattista G
Publication Date: 2021-12

Variant appearance in text: PKD1: 10720_10721insAGGG
PubMed Link: 33964006
Variant Present in the following documents:
  • Main text
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