Variant #0000147882 (NC_000011.9:g.88911139G>T, NM_000372.4:c.18G>T (TYR))

Chromosome 11
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.88911139G>T
DNA change (hg38) g.89177971G>T
Published as -
ISCN -
DB-ID TYR_000289
Variant remarks copied from the “Albanism Database” (University of Minnesota)
Reference Albinism Database
ClinVar ID -
dbSNP ID rs76180653
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner William (Bill) Oetting
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-12-04 10:04:54 +01:00 (CET)
Date last edited 2024-02-02 03:42:58 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 ?/? 1 c.18G>T r.(?) p.(Leu6Phe)


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