Variant #0000915176 (NC_000009.11:g.98244365A>C, NC_000009.11(NM_000264.3):c.655-43T>G (PTCH1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.98244365A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH1_000275
Frequency 1/13006
Freq. EA 1/8600
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 17:05:59 +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.655-43T>G r.(=) p.(=)