Variant #0000147739 (NC_000011.9:g.88911696C>A, NM_000372.4:c.575C>A (TYR))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.88911696C>A
DNA change (hg38) g.89178528C>A
Published as -
ISCN -
DB-ID TYR_000012 See all 165 reported entries
Variant remarks enzyme assay showed reduced (0.40) tyrosine hydroxylase and DOPA oxidase activities
Reference PubMed: Chaki 2011, Journal: Chanki 2001
ClinVar ID -
dbSNP ID rs1042602
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.25452 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 16:59:06 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +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.575C>A r.(?) p.Ser192Tyr


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