HR c.767G>T ;(p.G256V)

Variant ID: 8-21985188-C-A

NM_005144.4(HR):c.767G>T;(p.G256V)

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:

Nucleostemin deletion reveals an essential mechanism that maintains the genomic stability of stem and progenitor cells.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Meng, Lingjun L; Lin, Tao T; Peng, Guang G; Hsu, Joseph K JK; Lee, Sun S; Lin, Shiaw-Yih SY; Tsai, Robert Y L RY
Publication Date: 2013-07-09

Variant appearance in text: HR: G256V
PubMed Link: 23798389
Variant Present in the following documents:
  • Main text
View BVdb publication page