Variant #0000575447 (NC_000023.10:g.27998106C>T, NM_001017930.1:c.1346G>A (DCAF8L1))

Chromosome X
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.27998106C>T
DNA change (hg38) g.27979989C>T
Published as DCAF8L1(NM_001017930.1):c.1346G>A (p.R449Q), DCAF8L1(NM_001017930.2):c.1346G>A (p.(Arg449Gln))
ISCN -
DB-ID DCAF8L1_000017 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) 0.00011 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCAF8L1 NM_001017930.1 -?/. - c.1346G>A r.(?) p.(Arg449Gln)


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