RET c.2267C>A ;(p.A756D)

Variant ID: 10-43612162-C-A

NM_020975.4(RET):c.2267C>A;(p.A756D)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: RET: A756D
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page


Beyond KRAS: Practical Molecular Targets in Pancreatic Adenocarcinoma.

Case Reports In Oncology
Grinshpun, Albert A; Zarbiv, Yonaton Y; Roszik, Jason J; Subbiah, Vivek V; Hubert, Ayala A
Publication Date: 2019

Variant appearance in text: RET: A756D
PubMed Link: 30792639
Variant Present in the following documents:
  • Main text
View BVdb publication page