Variant #0000000111 (NC_000009.11:g.135939939A>C, NM_001807.4:c.224A>C (CEL))

Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.135939939A>C
Reference -
DB-ID CEL_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Sabine Heber
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Sabine Heber
Date created 2020-10-08 10:54:31 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEL NM_001807.4 +?/+? 2 c.224A>C r.(?) p.(Gln75Pro)