Variant #0000984903 (NC_000010.10:g.43606856G>A, NM_020975.4:c.1465G>A (RET))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.43606856G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RET_000088
Frequency 2/13006
Freq. EA 1/8600
Freq. AA 1/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:30:47 +02:00 (CEST)
Date last edited 2015-09-24 13:54:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RET NM_020975.4 ?/? c.1465G>A r.(?) p.(Asp489Asn)