Variant #0000000035 (NC_000007.13:g.130024398C>T, NM_001868.2:c.718C>T (CPA1))

Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.130024398C>T
Reference -
DB-ID CPA1_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2018-01-25 14:29:48 +00:00 (UTC)
Date last edited 2018-01-25 14:30:53 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPA1 NM_001868.2 ./+? 7 c.718C>T r.(?) p.(Arg240Trp)