TSC2 c.1415_1416del ;(p.V472Afs*9)

Variant ID: 16-2113023-TTG-T

NM_000548.3(TSC2):c.1415_1416del;(p.V472Afs*9)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing.

Plos Genetics
Tyburczy, Magdalena E ME; Dies, Kira A KA; Glass, Jennifer J; Camposano, Susana S; Chekaluk, Yvonne Y; Thorner, Aaron R AR; Lin, Ling L; Krueger, Darcy D; Franz, David N DN; Thiele, Elizabeth A EA; Sahin, Mustafa M; Kwiatkowski, David J DJ
Publication Date: 2015-11

Variant appearance in text: TSC2: 1413_1414delTG
PubMed Link: 26540169
Variant Present in the following documents:
  • Main text
  • pgen.1005637.pdf
  • pgen.1005637.s005.pdf
View BVdb publication page