Variant #0000864876 (NC_000016.9:g.66562930G>A, NM_004614.4:c.416C>T (TK2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66562930G>A
DNA change (hg38) -
Published as TK2(NM_001272050.2):c.125C>T (p.A42V), TK2(NM_004614.5):c.416C>T (p.A139V)
ISCN -
DB-ID TK2_000003 See all 3 reported entries
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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TK2 NM_001172643.1 +?/. - c.323C>T r.(?) p.(Ala108Val)
TK2 NM_001172644.1 +?/. - c.341C>T r.(?) p.(Ala114Val)
TK2 NM_004614.4 +?/. - c.416C>T r.(?) p.(Ala139Val)


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