RET c.2646A>C ;(p.V882=)

Variant ID: 10-43615567-A-C

NM_020975.4(RET):c.2646A>C;(p.V882=)

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:

Correlation of RET somatic mutations with clinicopathological features in sporadic medullary thyroid carcinomas.

British Journal Of Cancer
Moura, M M MM; Cavaco, B M BM; Pinto, A E AE; Domingues, R R; Santos, J R JR; Cid, M O MO; Bugalho, M J MJ; Leite, V V
Publication Date: 2009-06-02

Variant appearance in text: RET: Val882Val
PubMed Link: 19401695
Variant Present in the following documents:
  • Main text
  • 6605056a.pdf
View BVdb publication page