Variant #0000610169 (NC_000006.11:g.15524679G>A, NC_000006.11(NM_032122.4):c.811+78C>T (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.15524679G>A
DNA change (hg38) g.15524448G>A
Published as DTNBP1(NM_183040.2):c.889C>T (p.(His297Tyr))
ISCN -
DB-ID DTNBP1_000030 See all 2 reported entries
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) 0.01153 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 2019-12-04 15:24:38 +01:00 (CET)
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     
JARID2 NM_004973.3 -/. - c.*4197G>A r.(=) p.(=)
DTNBP1 NM_032122.4 -/. - c.811+78C>T r.(=) p.(=)


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