VCAN c.9686A>G ;(p.N3229S)

Variant ID: 5-82850808-A-G

NM_004385.4(VCAN):c.9686A>G;(p.N3229S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome sequencing in families with chronic central serous chorioretinopathy.

Molecular Genetics & Genomic Medicine
Schellevis, Rosa L RL; van Dijk, Elon H C EHC; Breukink, Myrte B MB; Keunen, Jan E E JEE; Santen, Gijs W E GWE; Hoyng, Carel B CB; de Jong, Eiko K EK; Boon, Camiel J F CJF; den Hollander, Anneke I AI
Publication Date: 2019-04

Variant appearance in text: VCAN: N3229S; rs768896921
PubMed Link: 30724488
Variant Present in the following documents:
  • MGG3-7-na-s005.xlsx, sheet 11
View BVdb publication page