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ATP2B2 c.1787del ;(p.L596Cfs*14)
Variant ID: 3-10401679-CA-C
NM_001001331.2(
ATP2B2
):c.1787del;(p.L596Cfs*14)
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:
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder.
Nature Communications
Nishioka, Masaki M; Kazuno, An-A AA; Nakamura, Takumi T; Sakai, Naomi N; Hayama, Takashi T; Fujii, Kumiko K; Matsuo, Koji K; Komori, Atsuko A; Ishiwata, Mizuho M; Watanabe, Yoshinori Y; Oka, Takashi T; Matoba, Nana N; Kataoka, Muneko M; Alkanaq, Ahmed N AN; Hamanaka, Kohei K; Tsuboi, Takashi T; Sengoku, Toru T; Ogata, Kazuhiro K; Iwata, Nakao N; Ikeda, Masashi M; Matsumoto, Naomichi N; Kato, Tadafumi T; Takata, Atsushi A
Publication Date: 2021-06-18
Variant appearance in text: ATP2B2: 1787delT; Leu596fs
PubMed Link:
34145229
Variant Present in the following documents:
41467_2021_23453_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page