KAT2A c.2302G>T ;(p.V768F)

Variant ID: 17-40266036-C-A

NM_021078.2(KAT2A):c.2302G>T;(p.V768F)

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: KAT2A: 2302G>T; Val768Phe
PubMed Link: 32473611
Variant Present in the following documents:
  • CAS-111-3000-s008.xls, sheet 1
View BVdb publication page