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MYCBPAP c.1385C>T ;(p.P462L)
Variant ID: 17-48600427-C-T
NM_032133.4(
MYCBPAP
):c.1385C>T;(p.P462L)
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:
Single-cell exome sequencing reveals multiple subclones in metastatic colorectal carcinoma.
Genome Medicine
Tang, Jie J; Tu, Kailing K; Lu, Keying K; Zhang, Jiaxun J; Luo, Kai K; Jin, Haoxuan H; Wang, Lei L; Yang, Lie L; Xiao, Weiran W; Zhang, Qilin Q; Liu, Xiaoling X; Ge, Xin Yi XY; Li, Guibo G; Zhou, Zongguang Z; Xie, Dan D
Publication Date: 2021-09-10
Variant appearance in text: MYCBPAP: P505L
PubMed Link:
34507604
Variant Present in the following documents:
13073_2021_962_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page
Genomic and transcriptomic profiling of carcinogenesis in patients with familial adenomatous polyposis.
Gut
Li, Jingyun J; Wang, Rui R; Zhou, Xin X; Wang, Wendong W; Gao, Shuai S; Mao, Yunuo Y; Wu, Xinglong X; Guo, Limei L; Liu, Haijing H; Wen, Lu L; Fu, Wei W; Tang, Fuchou F
Publication Date: 2020-07
Variant appearance in text: MYCBPAP: Pro505Leu
PubMed Link:
31744909
Variant Present in the following documents:
gutjnl-2019-319438supp006.xlsx, sheet 1
gutjnl-2019-319438supp006.xlsx, sheet 2
View BVdb publication page