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TSC2 c.1204_1206delinsAGC ;(p.G402S)
Variant ID: 16-2111956-GGG-AGC
NM_000548.3(
TSC2
):c.1204_1206delinsAGC;(p.G402S)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.
Hereditary Cancer In Clinical Practice
Wallander, Karin K; Thonberg, Håkan H; Nilsson, Daniel D; Tham, Emma E
Publication Date: 2021-10-28
Variant appearance in text: TSC2: Gly402Ser
PubMed Link:
34711244
Variant Present in the following documents:
Main text
View BVdb publication page
Autism throughout genetics: Perusal of the implication of ion channels.
Brain And Behavior
Daghsni, Marwa M; Rima, Mohamad M; Fajloun, Ziad Z; Ronjat, Michel M; Brusés, Juan L JL; M'rad, Ridha R; De Waard, Michel M
Publication Date: 2018-08
Variant appearance in text: TSC2: G402S
PubMed Link:
29934975
Variant Present in the following documents:
Main text
View BVdb publication page