Bibliome.ai browser hg19
Search
About
Stats
FAQ
TTN c.58464T>G ;(p.S19488R)
Variant ID: 2-179458563-A-C
NM_001267550.1(
TTN
):c.58464T>G;(p.S19488R)
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:
Genomic and Transcriptomic Characterization of Relapsed SCLC Through Rapid Research Autopsy.
Jto Clinical And Research Reports
Chen, Hui-Zi HZ; Bonneville, Russell R; Paruchuri, Anoosha A; Reeser, Julie W JW; Wing, Michele R MR; Samorodnitsky, Eric E; Krook, Melanie A MA; Smith, Amy M AM; Dao, Thuy T; Miya, Jharna J; Wang, Walter W; Yu, Lianbo L; Freud, Aharon G AG; Allenby, Patricia P; Cole, Sharon S; Otterson, Gregory G; Shields, Peter P; Carbone, David P DP; Roychowdhury, Sameek S
Publication Date: 2021-04
Variant appearance in text: TTN: S19488R
PubMed Link:
34590014
Variant Present in the following documents:
mmc8.xlsx, sheet 14
mmc8.xlsx, sheet 8
mmc8.xlsx, sheet 9
mmc8.xlsx, sheet 13
mmc8.xlsx, sheet 10
mmc8.xlsx, sheet 3
mmc8.xlsx, sheet 6
mmc14.xlsx, sheet 1
mmc8.xlsx, sheet 4
mmc13.xlsx, sheet 13
mmc8.xlsx, sheet 11
mmc8.xlsx, sheet 2
mmc8.xlsx, sheet 12
mmc8.xlsx, sheet 7
mmc8.xlsx, sheet 5
View BVdb publication page