Variant #0000527678 (NC_000006.11:g.15593332_15593333dup, NC_000006.11(NM_032122.4):c.489-9_489-8dup (DTNBP1))

Chromosome 6
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.15593332_15593333dup
DNA change (hg38) g.15593101_15593102dup
Published as DTNBP1(NM_183040.2):c.489-9_489-8dupTT
ISCN -
DB-ID DTNBP1_000026
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
DTNBP1 NM_032122.4 -/. - c.489-9_489-8dup r.(=) p.(=)


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