Variant #0000434766 (NC_000009.11:g.?, NM_000550.2:c.? (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.?
DNA change (hg38) -
Published as 844T>C (Ser243Ser)
ISCN -
DB-ID TYRP1_000003 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35866166
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
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)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYRP1 NM_000550.2 ?/? 4 c.? r.(?) p.(?)


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