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USH2A c.11598C>G ;(p.A3866=)
Variant ID: 1-215914830-G-C
NM_206933.2(
USH2A
):c.11598C>G;(p.A3866=)
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: USH2A: A3866A
PubMed Link:
34590014
Variant Present in the following documents:
mmc5.xlsx, sheet 8
mmc5.xlsx, sheet 7
mmc5.xlsx, sheet 5
mmc5.xlsx, sheet 10
mmc5.xlsx, sheet 4
mmc5.xlsx, sheet 9
mmc5.xlsx, sheet 2
mmc5.xlsx, sheet 11
mmc5.xlsx, sheet 6
mmc9.xlsx, sheet 2
mmc5.xlsx, sheet 13
mmc5.xlsx, sheet 3
View BVdb publication page