Variant #0000915198 (NC_000009.11:g.98248188G>C, NC_000009.11(NM_000264.3):c.395-32C>G (PTCH1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.98248188G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH1_000295
Frequency 7/13006
Freq. EA 0/8600
Freq. AA 7/4406
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 17:06:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PTCH1 NM_000264.3 ?/? c.395-32C>G r.(=) p.(=)