Bibliome.ai browser hg19
Search
About
Stats
FAQ
MED16 c.1141+12C>A
Variant ID: 19-881547-G-T
NM_005481.2(
MED16
):c.1141+12C>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:
Clonal lineage from normal endometrium to ovarian clear cell carcinoma through ovarian endometriosis.
Cancer Science
Suda, Kazuaki K; Cruz Diaz, Luis Antonio LA; Yoshihara, Kosuke K; Nakaoka, Hirofumi H; Yachida, Nozomi N; Motoyama, Teiichi T; Inoue, Ituro I; Enomoto, Takayuki T
Publication Date: 2020-08
Variant appearance in text: MED16: 1141+12C>A
PubMed Link:
32473611
Variant Present in the following documents:
CAS-111-3000-s008.xls, sheet 1
View BVdb publication page