HR c.2845_2846delinsCA ;(p.R949Q)

Variant ID: 8-21977617-CT-TG

NM_005144.4(HR):c.2845_2846delinsCA;(p.R949Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Thyroid Cancer: The Quest for Genetic Susceptibility Involving DNA Repair Genes.

Genes
Santos, Luís S LS; Gomes, Bruno Costa BC; Bastos, Hélder N HN; Gil, Octávia M OM; Azevedo, Ana Paula AP; Ferreira, Teresa C TC; Limbert, Edward E; Silva, Susana N SN; Rueff, José J
Publication Date: 2019-08-01

Variant appearance in text: HR: Arg949Gln
PubMed Link: 31374908
Variant Present in the following documents:
  • Main text
  • genes-10-00586.pdf
View BVdb publication page