Variant #0000558697 (NC_000016.9:g.66565330G>A, NM_004614.4:c.328C>T (TK2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66565330G>A
DNA change (hg38) g.66531427G>A
Published as TK2(NM_001271934.1):c.181C>T (p.Q61*)
ISCN -
DB-ID TK2_000016
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-09 17:45:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TK2 NM_001172643.1 +/. - c.235C>T r.(?) p.(Gln79Ter)
TK2 NM_001172644.1 +/. - c.253C>T r.(?) p.(Gln85Ter)
TK2 NM_004614.4 +/. - c.328C>T r.(?) p.(Gln110Ter)


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