Variant #0000000122 (NC_000002.11:g.189922152C>A, NM_000393.3:c.2231G>T (COL5A2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.189922152C>A
Reference -
DB-ID COL5A2_000001
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 2022-06-29 14:13:09 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL5A2 NM_000393.3 ./+? 34 c.2231G>T r.(?) p.(Gly744Val)