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CASP3 c.-16+2788G>A
Variant ID: 4-185566831-C-T
NM_004346.4(
CASP3
):c.-16+2788G>A
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:
Common variants in CASP3 confer susceptibility to Kawasaki disease.
Human Molecular Genetics
Onouchi, Yoshihiro Y; Ozaki, Kouichi K; Buns, Jane C JC; Shimizu, Chisato C; Hamada, Hiromichi H; Honda, Takafumi T; Terai, Masaru M; Honda, Akihito A; Takeuchi, Takashi T; Shibuta, Shoichi S; Suenaga, Tomohiro T; Suzuki, Hiroyuki H; Higashi, Kouji K; Yasukawa, Kumi K; Suzuki, Yoichi Y; Sasago, Kumiko K; Kemmotsu, Yasushi Y; Takatsuki, Shinichi S; Saji, Tsutomu T; Yoshikawa, Tetsushi T; Nagai, Toshiro T; Hamamoto, Kunihiro K; Kishi, Fumio F; Ouchi, Kazunobu K; Sato, Yoshitake Y; Newburger, Jane W JW; Baker, Annette L AL; Shulman, Stanford T ST; Rowley, Anne H AH; Yashiro, Mayumi M; Nakamura, Yoshikazu Y; Wakui, Keiko K; Fukushima, Yoshimitsu Y; Fujino, Akihiro A; Tsunoda, Tatsuhiko T; Kawasaki, Tomisaku T; Hata, Akira A; Nakamura, Yusuke Y; Tanaka, Toshihiro T
Publication Date: 2010-07-15
Variant appearance in text: rs4647616
PubMed Link:
20423928
Variant Present in the following documents:
Main text
View BVdb publication page