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TAGLN c.46T>G ;(p.S16A)
Variant ID: 11-117073775-T-G
NM_003186.3(
TAGLN
):c.46T>G;(p.S16A)
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:
Molecular subtypes of ALS are associated with differences in patient prognosis.
Nature Communications
Eshima, Jarrett J; O'Connor, Samantha A SA; Marschall, Ethan E; , ; Bowser, Robert R; Plaisier, Christopher L CL; Smith, Barbara S BS
Publication Date: 2023-01-06
Variant appearance in text: TAGLN: S16a
PubMed Link:
36609402
Variant Present in the following documents:
Main text
View BVdb publication page
nc886 is induced by TGF-β and suppresses the microRNA pathway in ovarian cancer.
Nature Communications
Ahn, Ji-Hye JH; Lee, Hyun-Sung HS; Lee, Ju-Seog JS; Lee, Yeon-Su YS; Park, Jong-Lyul JL; Kim, Seon-Young SY; Hwang, Jung-Ah JA; Kunkeaw, Nawapol N; Jung, Sung Yun SY; Kim, Tae Jin TJ; Lee, Kwang-Soo KS; Jeon, Sung Ho SH; Lee, Inhan I; Johnson, Betty H BH; Choi, Jung-Hye JH; Lee, Yong Sun YS
Publication Date: 2018-03-21
Variant appearance in text: TAGLN: S16A
PubMed Link:
29563500
Variant Present in the following documents:
41467_2018_3556_MOESM2_ESM.pdf
View BVdb publication page