RET c.808C>G ;(p.P270A)

Variant ID: 10-43600582-C-G

NM_020975.4(RET):c.808C>G;(p.P270A)

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:

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.

Kidney International
Hwang, Daw-Yang DY; Dworschak, Gabriel C GC; Kohl, Stefan S; Saisawat, Pawaree P; Vivante, Asaf A; Hilger, Alina C AC; Reutter, Heiko M HM; Soliman, Neveen A NA; Bogdanovic, Radovan R; Kehinde, Elijah O EO; Tasic, Velibor V; Hildebrandt, Friedhelm F
Publication Date: 2014-06

Variant appearance in text: RET: 808C>G; P270A
PubMed Link: 24429398
Variant Present in the following documents:
  • Main text
View BVdb publication page