Variant #0000434762 (NC_000009.11:g.12695756T>A, NM_000550.2:c.627T>A (TYRP1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.12695756T>A
DNA change (hg38) g.12695756T>A
Published as 627T>A (Gly209Gly)
ISCN -
DB-ID TYRP1_000002 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1800374
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner William (Bill) Oetting
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by William (Bill) Oetting
Date created 2011-10-18 16:27:13 +02:00 (CEST)
Date last edited 2021-09-09 14:41:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYRP1 NM_000550.2 ?/? 3 c.627T>A r.(?) p.(=)


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