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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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
View BVdb publication page