Variant #0000527675 (NC_000006.11:g.15523347C>T, NM_032122.4:c.915G>A (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.15523347C>T
DNA change (hg38) g.15523116C>T
Published as DTNBP1(NM_001271667.1):c.672G>A (p.S224=)
ISCN -
DB-ID DTNBP1_000023
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) 0.00019 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 14:43:34 +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.*2865C>T r.(=) p.(=)
DTNBP1 NM_032122.4 -?/. - c.915G>A r.(?) p.(Ser305=)


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