Variant #0000655517 (NC_000006.11:g.15523293_15523295del, NM_032122.4:c.972_974del (DTNBP1))

Chromosome 6
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.15523293_15523295del
DNA change (hg38) g.15523062_15523064del
Published as DTNBP1(NM_001271667.1):c.729_731delGGA (p.E244del)
ISCN -
DB-ID DTNBP1_000033
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JARID2 NM_004973.3 ?/. - c.*2811_*2813del r.(=) p.(=)
DTNBP1 NM_032122.4 ?/. - c.972_974del r.(?) p.(Glu325del)


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