Variant #0000275754 (NC_000006.11:g.15523242C>G, NM_032122.4:c.1020G>C (DTNBP1))

Chromosome 6
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.15523242C>G
DNA change (hg38) g.15523011C>G
Published as DTNBP1(NM_001271667.1):c.777G>C (p.E259D)
ISCN -
DB-ID DTNBP1_000003
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) 2.0E-5 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 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     
JARID2 NM_004973.3 -?/. - c.*2760C>G r.(=) p.(=)
DTNBP1 NM_032122.4 -?/. - c.1020G>C r.(?) p.(Glu340Asp)


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