GC c.10_15delinsC ;(p.V4Rfs*19)

Variant ID: 4-72649721-CAGGAC-G

NM_000583.3(GC):c.10_15delinsC;(p.V4Rfs*19)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Retinal Diseases Caused by Mutations in Genes Not Specifically Associated with the Clinical Diagnosis.

Plos One
Wang, Xia X; Feng, Yanming Y; Li, Jianli J; Zhang, Wei W; Wang, Jing J; Lewis, Richard A RA; Wong, Lee-Jun LJ
Publication Date: 2016

Variant appearance in text: GC: 9_15delinsGC
PubMed Link: 27788217
Variant Present in the following documents:
  • Main text
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