HR c.1385G>T ;(p.G462V)

Variant ID: 8-21984570-C-A

NM_005144.4(HR):c.1385G>T;(p.G462V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.

Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31

Variant appearance in text: HR: G462V
PubMed Link: 33384420
Variant Present in the following documents:
  • Main text
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