Variant #0000147748 (NC_000011.9:g.89018011G>A, NM_000372.4:c.1255G>A (TYR))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.89018011G>A
DNA change (hg38) g.89284843G>A
Published as -
ISCN -
DB-ID TYR_000020 See all 19 reported entries
Variant remarks enzyme assay showed no tyrosine hydroxylase and DOPA oxidase activities, ER retention protein
Reference PubMed: Chaki 2011, Journal: Chanki 2001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-12-02 17:23:41 +01:00 (CET)
Date last edited 2025-03-13 01:52:09 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 +/. 4 c.1255G>A r.(?) p.Gly419Arg


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