Variant #0000147744 (NC_000011.9:g.88911393G>C, NM_000372.4:c.272G>C (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.88911393G>C
DNA change (hg38) g.89178225G>C
Published as -
ISCN -
DB-ID TYR_000016 See all 3 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) Retrieve
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 2025-06-12 10:16:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 +/. 1 c.272G>C r.(?) p.Cys91Ser


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