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CPAMD8 c.1193T>G ;(p.V398G)
Variant ID: 19-17104299-A-C
NM_015692.2(
CPAMD8
):c.1193T>G;(p.V398G)
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:
Exomic sequencing of four rare central nervous system tumor types.
Oncotarget
Bettegowda, Chetan C; Agrawal, Nishant N; Jiao, Yuchen Y; Wang, Yuxuan Y; Wood, Laura D LD; Rodriguez, Fausto J FJ; Hruban, Ralph H RH; Gallia, Gary L GL; Binder, Zev A ZA; Riggins, Callen J CJ; Salmasi, Vafi V; Riggins, Gregory J GJ; Reitman, Zachary J ZJ; Rasheed, Ahmed A; Keir, Stephen S; Shinjo, Sueli S; Marie, Suely S; McLendon, Roger R; Jallo, George G; Vogelstein, Bert B; Bigner, Darell D; Yan, Hai H; Kinzler, Kenneth W KW; Papadopoulos, Nickolas N
Publication Date: 2013-04
Variant appearance in text: CPAMD8: V445G
PubMed Link:
23592488
Variant Present in the following documents:
oncotarget-04-572-s001.xlsx, sheet 4
View BVdb publication page