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UGT2B10 c.819T>A ;(p.V273=)
Variant ID: 4-69683847-T-A
NM_001075.4(
UGT2B10
):c.819T>A;(p.V273=)
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:
Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.
Plos One
PatiƱo, Liliana Catherine LC; Battu, Rajani R; Ortega-Recalde, Oscar O; Nallathambi, Jeyabalan J; Anandula, Venkata Ramana VR; Renukaradhya, Umashankar U; Laissue, Paul P
Publication Date: 2014
Variant appearance in text: UGT2B10: V273V
PubMed Link:
25333361
Variant Present in the following documents:
pone.0109576.s002.xls, sheet 3
View BVdb publication page