FOXD4 c.1025C>T ;(p.P342L)

Variant ID: 9-117095-G-A

NM_207305.4(FOXD4):c.1025C>T;(p.P342L)

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: FOXD4: P342L
PubMed Link: 31139268
Variant Present in the following documents:
  • 13053_2019_112_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page