Variant #0000139568 (NC_000001.10:g.161293496T>A, NC_000001.10(NM_003001.3):c.77+36T>A (SDHC))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.161293496T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SDHC_000016
Frequency 447/12988
Freq. EA 179/8600
Freq. AA 268/4388
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 20:06:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SDHC NM_003001.3 ?/? c.77+36T>A r.(=) p.(=)