RET c.718G>C ;(p.V240L)

Variant ID: 10-43600492-G-C

NM_020975.4(RET):c.718G>C;(p.V240L)

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:

Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated Hypercalcemia.

Hormones & Cancer
Khairi, Shafaq S; Osborne, Jenae J; Jacobs, Michelle F MF; Clines, Gregory T GT; Miller, Barbra S BS; Hughes, David T DT; Else, Tobias T
Publication Date: 2020-10

Variant appearance in text: RET: 718G>C; Val240Leu
PubMed Link: 32761341
Variant Present in the following documents:
  • Main text
View BVdb publication page