Variant #0000984853 (NC_000010.10:g.43600492G>C, NM_020975.4:c.718G>C (RET))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.43600492G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RET_000039
Frequency 1/12996
Freq. EA 1/8594
Freq. AA 0/4402
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 2013-05-04 19:14:11 +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.718G>C r.(?) p.(Val240Leu)