Variant #0000863832 (NC_000015.9:g.43028912G>A, NM_173500.3:c.*9081C>T (TTBK2))

Chromosome 15
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.43028912G>A
DNA change (hg38) -
Published as CDAN1(NM_138477.2):c.157C>T (p.(Leu53=))
ISCN -
DB-ID CDAN1_000030
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) 0.01071 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDAN1 NM_138477.2 -?/. - c.157C>T r.(?) p.(Leu53=)
TTBK2 NM_173500.3 -?/. - c.*9081C>T r.(=) p.(=)


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