Variant #0000000496 (NC_000007.13:g.142458412C>T, NM_002769.4:c.47C>T (PRSS1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.142458412C>T
Reference -
DB-ID PRSS1_000002
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-05-07 12:21:38 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRSS1 NM_002769.4 +/+ 2 c.47C>T r.(?) p.(Ala16Val)