Variant #0000065241 (NC_000001.10:g.45296711G>A, NM_003738.4:c.622C>T (PTCH2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.45296711G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH2_000228
Frequency 18/13006
Freq. EA 0/8600
Freq. AA 18/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 18:29:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTCH2 NM_003738.4 ?/? c.622C>T r.(?) p.(Arg208Cys)