Variant #0000065266 (NC_000001.10:g.45298040G>C, NC_000001.10(NM_003738.4):c.266-27C>G (PTCH2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.45298040G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH2_000243
Frequency 5/13006
Freq. EA 0/8600
Freq. AA 5/4406
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 18:29:59 +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.266-27C>G r.(=) p.(=)