PKD1 c.4664C>G ;(p.A1555G)

Variant ID: 16-2160504-G-C

NM_001009944.2(PKD1):c.4664C>G;(p.A1555G)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Human iPSC banking: barriers and opportunities.

Journal Of Biomedical Science
Huang, Ching-Ying CY; Liu, Chun-Lin CL; Ting, Chien-Yu CY; Chiu, Yueh-Ting YT; Cheng, Yu-Che YC; Nicholson, Martin W MW; Hsieh, Patrick C H PCH
Publication Date: 2019-10-28

Variant appearance in text: PKD1: A1555G
PubMed Link: 31660969
Variant Present in the following documents:
  • 12929_2019_Article_578.pdf
View BVdb publication page



Genome sequencing and implications for rare disorders.

Orphanet Journal Of Rare Diseases
Posey, Jennifer E JE
Publication Date: 2019-06-24

Variant appearance in text: PKD1: A1555G
PubMed Link: 31234920
Variant Present in the following documents:
  • 13023_2019_Article_1127.pdf
View BVdb publication page



Clinical and public health implications of emerging genetic technologies.

Seminars In Nephrology
Laberge, Anne-Marie AM; Burke, Wylie W
Publication Date: 2010-03

Variant appearance in text: PKD1: A1555G
PubMed Link: 20347647
Variant Present in the following documents:
  • Main text
View BVdb publication page