RET c.1495C>T ;(p.Q499*)

Variant ID: 10-43606886-C-T

NM_020975.4(RET):c.1495C>T;(p.Q499*)

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:

An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticist.

American Journal Of Medical Genetics. Part C, Seminars In Medical Genetics
Mena, Rafael R; Mendoza, Esperanza E; Gomez Peña, Maria M; Valencia, C Alexander CA; Ullah, Ehsan E; Hufnagel, Robert B RB; Prada, Carlos E CE
Publication Date: 2020-12

Variant appearance in text: RET: 1495C>T; Gln499*
PubMed Link: 33219631
Variant Present in the following documents:
  • Main text
View BVdb publication page