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RARA c.745T>C ;(p.F249L)
Variant ID: 17-38508697-T-C
NM_000964.3(
RARA
):c.745T>C;(p.F249L)
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:
Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma.
Molecular Vision
Jiang, Dan D; Yang, Zhikuan Z; Li, Shiqiang S; Xiao, Xueshan X; Jia, Xiaoyun X; Wang, Panfeng P; Guo, Xiangming X; Liu, Xing X; Zhang, Qingjiong Q
Publication Date: 2013
Variant appearance in text: RARA: Phe249Leu
PubMed Link:
24227917
Variant Present in the following documents:
mv-v19-2217.pdf
View BVdb publication page