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RET c.352del ;(p.L118Cfs*106)
Variant ID: 10-43597800-TC-T
NM_020975.4(
RET
):c.352del;(p.L118Cfs*106)
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:
SLIT2/ROBO1-miR-218-1-RET/PLAG1: a new disease pathway involved in Hirschsprung's disease.
Journal Of Cellular And Molecular Medicine
Tang, Weibing W; Tang, Junwei J; He, Jun J; Zhou, Zhigang Z; Qin, Yufeng Y; Qin, Jingjing J; Li, Bo B; Xu, Xiaoqun X; Geng, Qiming Q; Jiang, Weiwei W; Wu, Wei W; Wang, Xinru X; Xia, Yankai Y
Publication Date: 2015-06
Variant appearance in text: RET: 352delC
PubMed Link:
25786906
Variant Present in the following documents:
Main text
jcmm0019-1197.pdf
View BVdb publication page