Variant #0000807500 (NC_000016.9:g.66575772G>A, NC_000016.9(NM_004614.4):c.231+10C>T (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.66575772G>A
DNA change (hg38) -
Published as TK2(NM_001271934.1):c.84+10C>T, TK2(NM_001271934.2):c.84+10C>T
ISCN -
DB-ID TK2_000010 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) 0.00528 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.138+10C>T r.(=) p.(=)
TK2 NM_001172644.1 -?/. - c.157-4852C>T r.(=) p.(=)
TK2 NM_004614.4 -?/. - c.231+10C>T r.(=) p.(=)


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