TSC2 c.3883+6G>A

Variant ID: 16-2132511-G-A

NM_000548.3(TSC2):c.3883+6G>A

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:

A Pilot Study of Clinical Targeted Next Generation Sequencing for Prostate Cancer: Consequences for Treatment and Genetic Counseling.

The Prostate
Cheng, Heather H HH; Klemfuss, Nola N; Montgomery, Bruce B; Higano, Celestia S CS; Schweizer, Michael T MT; Mostaghel, Elahe A EA; McFerrin, Lisa G LG; Yu, Evan Y EY; Nelson, Peter S PS; Pritchard, Colin C CC
Publication Date: 2016-10

Variant appearance in text: TSC2: 3883+6G>A
PubMed Link: 27324988
Variant Present in the following documents:
  • Main text
View BVdb publication page