Variant #0000981208 (NC_000015.9:g.43028278T>G, NM_173500.3:c.*9715A>C (TTBK2))

Chromosome 15
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.43028278T>G
DNA change (hg38) -
Published as CDAN1(NM_138477.4):c.570-2A>C
ISCN -
DB-ID CDAN1_000031
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDAN1 NM_138477.2 ?/. - c.570-2A>C r.spl? p.?
TTBK2 NM_173500.3 ?/. - c.*9715A>C r.(=) p.(=)


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