CCDC110 c.1987G>T ;(p.E663*)

Variant ID: 4-186379754-C-A

NM_152775.3(CCDC110):c.1987G>T;(p.E663*)

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:

Endometrioid endometrial cancer "recurring" as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?

Hereditary Cancer In Clinical Practice
Jiang, Wei W; Gao, Tong T; Tao, Xiang X; Zhu, Menghan M; Yao, Liangqing L; Feng, Weiwei W
Publication Date: 2019

Variant appearance in text: CCDC110: E663X
PubMed Link: 31139268
Variant Present in the following documents:
  • 13053_2019_112_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page