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TSC2 c.2355+2T>A
Variant ID: 16-2122986-T-A
NM_000548.3(
TSC2
):c.2355+2T>A
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:
Cortical Dysplasia and the mTOR Pathway: How the Study of Human Brain Tissue Has Led to Insights into Epileptogenesis.
International Journal Of Molecular Sciences
Lee, Wei Shern WS; Baldassari, Sara S; Stephenson, Sarah E M SEM; Lockhart, Paul J PJ; Baulac, Stéphanie S; Leventer, Richard J RJ
Publication Date: 2022-01-25
Variant appearance in text: TSC2: 2355+2T>A
PubMed Link:
35163267
Variant Present in the following documents:
Main text
ijms-23-01344.pdf
View BVdb publication page
Cortical Dysplasia and the mTOR Pathway: How the Study of Human Brain Tissue Has Led to Insights into Epileptogenesis.
International Journal Of Molecular Sciences
Lee, Wei Shern WS; Baldassari, Sara S; Stephenson, Sarah E M SEM; Lockhart, Paul J PJ; Baulac, Stéphanie S; Leventer, Richard J RJ
Publication Date: 2022-01-25
Variant appearance in text: TSC2: 2355+2T>A
PubMed Link:
35163267
Variant Present in the following documents:
Main text
ijms-23-01344.pdf
View BVdb publication page