Variant #0000915138 (NC_000009.11:g.98241268G>A, NC_000009.11(NM_000264.3):c.1215+14C>T (PTCH1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.98241268G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PTCH1_000235
Frequency 2/13006
Freq. EA 2/8600
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 17:05:54 +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.1215+14C>T r.(=) p.(=)