Variant #0000807822 (NC_000007.13:g.155598978G>T, NC_000007.13(NM_000193.2):c.562+12C>A (SHH))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.155598978G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SHH_000010
Frequency 1/12992
Freq. EA 1/8588
Freq. AA 0/4404
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SHH NM_000193.2 ?/? c.562+12C>A r.(=) p.(=)