Variant #0000558696 (NC_000016.9:g.66551716T>C, NM_004614.4:c.514A>G (TK2))

Chromosome 16
Allele Unknown
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.66551716T>C
DNA change (hg38) g.66517813T>C
Published as TK2(NM_001172643.1):c.421A>G (p.(Met141Val))
ISCN -
DB-ID TK2_000015
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TK2 NM_001172643.1 -?/. - c.421A>G r.(?) p.(Met141Val)
TK2 NM_001172644.1 -?/. - c.439A>G r.(?) p.(Met147Val)
TK2 NM_004614.4 -?/. - c.514A>G r.(?) p.(Met172Val)


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