Variant #0000807823 (NC_000007.13:g.155599064C>T, NM_000193.2:c.488G>A (SHH))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.155599064C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SHH_000011
Frequency 2/13004
Freq. EA 2/8598
Freq. AA 0/4406
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 16:28:58 +02:00 (CEST)
Date last edited 2013-05-04 13:57:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SHH NM_000193.2 ?/? c.488G>A r.(?) p.(Arg163His)