Variant #0000065217 (NC_000001.10:g.45295260del, NC_000001.10(NM_003738.4):c.1083+26del (PTCH2))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.45295260del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH2_000267
Frequency 17/12520
Freq. EA 12/8254
Freq. AA 5/4266
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 2013-08-22 17:40:09 +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.1083+26del r.(=) p.(=)