NF1 c.6642+2T>C

Variant ID: 17-29664602-T-C

NM_001042492.2(NF1):c.6642+2T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A comprehensive next generation sequencing tissue assay for Asian-prevalent cancers-Analytical validation and performance evaluation with clinical samples.

Frontiers In Molecular Biosciences
Ng, Cedric Chuan-Young CC; Lim, Sandy S; Lim, Abner Herbert AH; Md Nasir, Nur Diyana ND; Zhang, Jingxian J; Rajasegaran, Vikneswari V; Lee, Jing Yi JY; Kok, Jessica Sook Ting JST; Thike, Aye Aye AA; Lim, Johnathan Xiande JX; Weng, Ruifen R; Yee, Sidney S; Choudhury, Yukti Y; Chan, Jason Yongsheng JY; Tan, Puay Hoon PH; Tan, Min-Han MH; Teh, Bin Tean BT
Publication Date: 2022

Variant appearance in text: NF1: 6642+2T>C
PubMed Link: 36213130
Variant Present in the following documents:
  • DataSheet1.xlsx, sheet 4
View BVdb publication page