Variant #0000867297 (NC_000023.10:g.27765423_27765446del, NM_001136533.1:c.411_434del (DCAF8L2))

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.27765423_27765446del
DNA change (hg38) -
Published as DCAF8L2(NM_001353448.1):c.411_434delGGAGGAGGAGGAGGAGGAGGAGGA (p.E140_E147del)
ISCN -
DB-ID DCAF8L2_000024
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCAF8L2 NM_001136533.1 ?/. - c.411_434del r.(?) p.(Glu140_Glu147del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.