Variant #0000858467 (NC_000002.11:g.25967172_25967177dup, NM_018263.4:c.2031_2036dup (ASXL2))

Chromosome 2
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.25967172_25967177dup
DNA change (hg38) -
Published as ASXL2(NM_018263.5):c.2031_2036dupCGCCGC (p.A683_A684dup)
ISCN -
DB-ID ASXL2_000032
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 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASXL2 NM_018263.4 ?/. - c.2031_2036dup r.(?) p.(Ala683_Ala684dup)


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