Variant #0000666093 (NC_000012.11:g.98928103C>T, NM_003276.2:c.2068C>T (TMPO))

Chromosome 12
Allele Both (homozygous)
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.98928103C>T
DNA change (hg38) g.98534325C>T
Published as -
ISCN -
DB-ID TMPO_000051 See all 3 reported entries
Variant remarks allele frequency 0.015 ExAC database (February, 2017), identified in 141 homozygotes
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01865 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-05-19 15:06:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMPO NM_003276.2 -?/. - c.2068C>T r.(?) p.(Arg690Cys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.