Variant #0000309202 (NC_000016.9:g.66545982C>T, NC_000016.9(NM_004614.4):c.700-13G>A (TK2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66545982C>T
DNA change (hg38) g.66512079C>T
Published as TK2(NM_001271934.2):c.553-13G>A
ISCN -
DB-ID TK2_000008 See all 2 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) 0.11261 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.607-13G>A r.(=) p.(=)
TK2 NM_001172644.1 -/. - c.625-13G>A r.(=) p.(=)
TK2 NM_004614.4 -/. - c.700-13G>A r.(=) p.(=)


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