TSC2 c.199G>T ;(p.V67F)

Variant ID: 16-2100461-G-T

NM_000548.3(TSC2):c.199G>T;(p.V67F)

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 the Germline Mutation Profile in Esophageal Squamous Cell Carcinoma by Whole Exome Sequencing.

Frontiers In Genetics
Deng, Jiaying J; Weng, Xiaoling X; Ye, Junyi J; Zhou, Daizhan D; Liu, Yun Y; Zhao, Kuaile K
Publication Date: 2019

Variant appearance in text: TSC2: Val67Phe
PubMed Link: 30833958
Variant Present in the following documents:
  • Main text
  • fgene-10-00047.pdf
View BVdb publication page