Variant #0000247383 (NC_000016.9:g.66582866A>G, NC_000016.9(NM_004614.4):c.156+15T>C (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.66582866A>G
DNA change (hg38) g.66548963A>G
Published as TK2(NM_001271934.2):c.-87+15T>C
ISCN -
DB-ID TK2_000011
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) 0.01495 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.63+15T>C r.(=) p.(=)
TK2 NM_001172644.1 -/. - c.156+15T>C r.(=) p.(=)
CKLF-CMTM1 NM_001202509.1 -/. - c.-3753A>G r.(?) p.(=)
TK2 NM_004614.4 -/. - c.156+15T>C r.(=) p.(=)
CKLF NM_016326.3 -/. - c.-3753A>G r.(?) p.(=)
CMTM1 NM_052999.3 -/. - c.-17551A>G r.(?) p.(=)


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