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TTC14 c.465T>G ;(p.D155E)
Variant ID: 3-180321090-T-G
NM_133462.3(
TTC14
):c.465T>G;(p.D155E)
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:
Exome-wide Association Study Identifies CLEC3B Missense Variant p.S106G as Being Associated With Extreme Longevity in East Asian Populations.
The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Tanisawa, Kumpei K; Arai, Yasumichi Y; Hirose, Nobuyoshi N; Shimokata, Hiroshi H; Yamada, Yoshiji Y; Kawai, Hisashi H; Kojima, Motonaga M; Obuchi, Shuichi S; Hirano, Hirohiko H; Yoshida, Hideyo H; Suzuki, Hiroyuki H; Fujiwara, Yoshinori Y; Ihara, Kazushige K; Sugaya, Maki M; Arai, Tomio T; Mori, Seijiro S; Sawabe, Motoji M; Sato, Noriko N; Muramatsu, Masaaki M; Higuchi, Mitsuru M; Liu, Yao-Wen YW; Kong, Qing-Peng QP; Tanaka, Masashi M
Publication Date: 2017-03-01
Variant appearance in text: TTC14: D155E; rs145653627
PubMed Link:
27154906
Variant Present in the following documents:
glw074_suppl_20160228_jgbs_2015_218r1_supplemantary_tables.xlsx, sheet 1
glw074_suppl_20160228_jgbs_2015_218r1_supplemantary_tables.xlsx, sheet 2
View BVdb publication page