WARS2 c.649G>C ;(p.V217L)

Variant ID: 1-119575968-C-G

NM_015836.3(WARS2):c.649G>C;(p.V217L)

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:

Identification of second primary tumors from lung metastases in patients with esophageal squamous cell carcinoma using whole-exome sequencing.

Theranostics
Xue, Liyan L; Li, Weihua W; Fan, Xinyi X; Zhao, Zitong Z; Zhou, Wei W; Feng, Zhimin Z; Liu, Linxiu L; Lin, Hua H; Li, Lin L; Xue, Xuemin X; Huang, Xuanlin X; Huang, Peide P; Guo, Jia J; Du, Peina P; Lu, Ning N; Li, Lin L; Zhan, Qimin Q; Song, Yongmei Y
Publication Date: 2020

Variant appearance in text: WARS2: 649G>C; Val217Leu
PubMed Link: 32929369
Variant Present in the following documents:
  • thnov10p10606s2.xls, sheet 3
View BVdb publication page