Variant #0000147862 (NC_000011.9:g.88911169C>T, NM_000372.4:c.48C>T (TYR))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88911169C>T
DNA change (hg38) g.89178001C>T
Published as -
ISCN -
DB-ID TYR_000293
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs148710429
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner William (Bill) Oetting
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-12-03 15:10:32 +01:00 (CET)
Date last edited 2022-10-13 05:07:44 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 -/- 1 c.48C>T r.(?) p.(Ser16=)


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