DLC1 c.265G>A ;(p.D89N)

Variant ID: 8-13357316-C-T

NM_182643.2(DLC1):c.265G>A;(p.D89N)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Systematic review and meta-analysis of genomic alterations in acral melanoma.

Pigment Cell & Melanoma Research
Broit, Natasa N; Johansson, Peter A PA; Rodgers, Chloe B CB; Walpole, Sebastian T ST; Hayward, Nicholas K NK; Pritchard, Antonia L AL
Publication Date: 2022-05

Variant appearance in text: DLC1: 265G>A; Asp89Asn
PubMed Link: 35229492
Variant Present in the following documents:
  • PCMR-35-369-s003.xlsx, sheet 6
View BVdb publication page



Integrated exome and RNA sequencing of TFE3-translocation renal cell carcinoma.

Nature Communications
Sun, Guangxi G; Chen, Junru J; Liang, Jiayu J; Yin, Xiaoxue X; Zhang, Mengni M; Yao, Jin J; He, Ning N; Armstrong, Cameron M CM; Zheng, Linmao L; Zhang, Xingming X; Zhu, Sha S; Sun, Xiaomeng X; Yang, Xiaoxia X; Zhao, Wanbin W; Liao, Banghua B; Pan, Xiuyi X; Nie, Ling L; Yang, Ling L; Chen, Yuntian Y; Zhao, Jinge J; Zhang, Haoran H; Dai, Jindong J; Shen, Yali Y; Liu, Jiyan J; Huang, Rui R; Liu, Jiandong J; Wang, Zhipeng Z; Ni, Yuchao Y; Wei, Qiang Q; Li, Xiang X; Zhou, Qiao Q; Huang, Haojie H; Liu, Zhenhua Z; Shen, Pengfei P; Chen, Ni N; Zeng, Hao H
Publication Date: 2021-09-06

Variant appearance in text: DLC1: 265G>A; D89N; rs150090193
PubMed Link: 34489456
Variant Present in the following documents:
  • 41467_2021_25618_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



Identification of potentially oncogenic alterations from tumor-only samples reveals Fanconi anemia pathway mutations in bladder carcinomas.

Npj Genomic Medicine
Madubata, Chioma J CJ; Roshan-Ghias, Alireza A; Chu, Timothy T; Resnick, Samuel S; Zhao, Junfei J; Arnes, Luis L; Wang, Jiguang J; Rabadan, Raul R
Publication Date: 2017

Variant appearance in text: rs150090193
PubMed Link: 29263839
Variant Present in the following documents:
  • 41525_2017_32_MOESM8_ESM.xlsx, sheet 4
View BVdb publication page



Uncovering the rare variants of DLC1 isoform 1 and their functional effects in a Chinese sporadic congenital heart disease cohort.

Plos One
Lin, Bin B; Wang, Yufeng Y; Wang, Zhen Z; Tan, Huilian H; Kong, Xianghua X; Shu, Yang Y; Zhang, Yuchao Y; Huang, Yun Y; Zhu, Yufei Y; Xu, Heng H; Wang, Zhiqiang Z; Wang, Ping P; Ning, Guang G; Kong, Xiangyin X; Hu, Guohong G; Hu, Landian L
Publication Date: 2014

Variant appearance in text: rs150090193
PubMed Link: 24587289
Variant Present in the following documents:
View BVdb publication page