Bibliome.ai browser hg19
Search
About
Stats
FAQ
TSC2 c.4744_4746del ;(p.I1582del)
Variant ID: 16-2136272-CTCA-C
NM_000548.3(
TSC2
):c.4744_4746del;(p.I1582del)
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:
Next-Generation Sequencing in Korean Children With Autism Spectrum Disorder and Comorbid Epilepsy.
Frontiers In Pharmacology
Lee, Junghan J; Ha, Sungji S; Lee, Seung-Tae ST; Park, Sung-Gyun SG; Shin, Saeam S; Choi, Jong Rak JR; Cheon, Keun-Ah KA
Publication Date: 2020
Variant appearance in text: TSC2: 4744_4746del; Ile1582del
PubMed Link:
32477112
Variant Present in the following documents:
Main text
fphar-11-00585.pdf
View BVdb publication page