SI c.1528_1529delinsCT ;(p.S510L)

Variant ID: 3-164767647-GA-AG

NM_001041.3(SI):c.1528_1529delinsCT;(p.S510L)

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:

CRY2 missense mutations suppress P53 and enhance cell growth.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Chan, Alanna B AB; Parico, Gian Carlo G GCG; Fribourgh, Jennifer L JL; Ibrahim, Lara H LH; Bollong, Michael J MJ; Partch, Carrie L CL; Lamia, Katja A KA
Publication Date: 2021-07-06

Variant appearance in text: SI: S510L
PubMed Link: 34183418
Variant Present in the following documents:
  • Main text
View BVdb publication page