Variant #0000558699 (NC_000016.9:g.66570874T>C, NM_004614.4:c.278A>G (TK2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66570874T>C
DNA change (hg38) g.66536971T>C
Published as TK2(NM_001271934.2):c.131A>G (p.N44S)
ISCN -
DB-ID TK2_000018
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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TK2 NM_001172643.1 ?/. - c.185A>G r.(?) p.(Asn62Ser)
TK2 NM_001172644.1 ?/. - c.203A>G r.(?) p.(Asn68Ser)
TK2 NM_004614.4 ?/. - c.278A>G r.(?) p.(Asn93Ser)


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