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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