Variant #0000065247 (NC_000001.10:g.45297507A>C, NC_000001.10(NM_003738.4):c.526-38T>G (PTCH2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.45297507A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH2_000234
Frequency 52/13002
Freq. EA 50/8596
Freq. AA 2/4406
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTCH2 NM_003738.4 ?/? c.526-38T>G r.(=) p.(=)