Variant #0000915161 (NC_000009.11:g.98242735G>A, NM_000264.3:c.882C>T (PTCH1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.98242735G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH1_000258
Frequency 3/13006
Freq. EA 3/8600
Freq. AA 0/4406
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 16:29:58 +02:00 (CEST)
Date last edited 2013-05-04 17:05:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTCH1 NM_000264.3 ?/? c.882C>T r.(=) p.(=)