PKD1 c.9313C>T ;(p.R3105W)

Variant ID: 16-2152146-G-A

NM_001009944.2(PKD1):c.9313C>T;(p.R3105W)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Autosomal Dominant Polycystic Kidney Disease: Presence of Hypomorphic Alleles in PKD1 Gene.

Indian Journal Of Nephrology
Pandita, S S; Khullar, D D; Saxena, R R; Verma, I C IC
Publication Date: 2018

Variant appearance in text: PKD1: Arg3105Trp
PubMed Link: 30647506
Variant Present in the following documents:
  • Main text
View BVdb publication page



Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.

Kidney International
Rossetti, Sandro S; Kubly, Vickie J VJ; Consugar, Mark B MB; Hopp, Katharina K; Roy, Sushmita S; Horsley, Sharon W SW; Chauveau, Dominique D; Rees, Lesley L; Barratt, T Martin TM; van't Hoff, William G WG; Niaudet, Patrick P; Niaudet, W Patrick WP; Torres, Vicente E VE; Harris, Peter C PC
Publication Date: 2009-04

Variant appearance in text: PKD1: R3105W
PubMed Link: 19165178
Variant Present in the following documents:
  • Main text
View BVdb publication page