Variant #0000434768 (NC_000009.11:g.12702279G>A, NM_000550.2:c.922G>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.12702279G>A
DNA change (hg38) g.12702279G>A
Published as D308N
ISCN -
DB-ID TYRP1_000005
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs41306053
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYRP1 NM_000550.2 ?/? 5 c.922G>A r.(?) p.(Asp308Asn)


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