RB1 c.1900T>C ;(p.S634P)

Variant ID: 13-49030425-T-C

NM_000321.2(RB1):c.1900T>C;(p.S634P)

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:

Understanding protein structural changes for oncogenic missense variants.

Heliyon
Hernandez, Rolando R; Facelli, Julio C JC
Publication Date: 2021-01

Variant appearance in text: RB1: Ser634Pro
PubMed Link: 33553733
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page