PARD3 c.3208C>G ;(p.R1070G)

Variant ID: 10-34558796-G-C

NM_001184785.1(PARD3):c.3208C>G;(p.R1070G)

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:

Exploring prognostic indicators in the pathological images of ovarian cancer based on a deep survival network.

Frontiers In Genetics
Wu, Meixuan M; Zhu, Chengguang C; Yang, Jiani J; Cheng, Shanshan S; Yang, Xiaokang X; Gu, Sijia S; Xu, Shilin S; Wu, Yongsong Y; Shen, Wei W; Huang, Shan S; Wang, Yu Y
Publication Date: 2022

Variant appearance in text: PARD3: 3208C>G; R1070G
PubMed Link: 36685892
Variant Present in the following documents:
  • Table3.xlsx, sheet 1
View BVdb publication page