Variant #0000728802 (NC_000023.10:g.27999120_27999131dup, NM_001017930.1:c.332_343dup (DCAF8L1))

Chromosome X
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.27999120_27999131dup
DNA change (hg38) -
Published as DCAF8L1(NM_001017930.1):c.332_343dupGGGAGGAGGAAG (p.G111_E114dup)
ISCN -
DB-ID DCAF8L1_000022
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 2021-02-08 18:36:18 +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     
DCAF8L1 NM_001017930.1 ?/. - c.332_343dup r.(?) p.(Gly111_Glu114dup)


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