ABCA4 c.2469C>A ;(p.N823K)

Variant ID: 1-94520785-G-T

NM_000350.2(ABCA4):c.2469C>A;(p.N823K)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Sheppard, Sarah S; Biswas, Sawona S; Li, Mindy H MH; Jayaraman, Vijayakumar V; Slack, Ian I; Romasko, Edward J EJ; Sasson, Ariella A; Brunton, Joshua J; Rajagopalan, Ramakrishnan R; Sarmady, Mahdi M; Abrudan, Jenica L JL; Jairam, Sowmya S; DeChene, Elizabeth T ET; Ying, Xiahoan X; Choi, Jiwon J; Wilkens, Alisha A; Raible, Sarah E SE; Scarano, Maria I MI; Santani, Avni A; Pennington, Jeffrey W JW; Luo, Minjie M; Conlin, Laura K LK; Devkota, Batsal B; Dulik, Matthew C MC; Spinner, Nancy B NB; Krantz, Ian D ID
Publication Date: 2018-12

Variant appearance in text: ABCA4: 2469C>A; Asn823Lys
PubMed Link: 29907799
Variant Present in the following documents:
  • Main text
  • 41436_2018_Article_4.pdf
View BVdb publication page