Variant #0000564671 (NC_000018.9:g.31322918C>T, NM_030632.1:c.3106C>T (ASXL3))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31322918C>T
DNA change (hg38) g.33742954C>T
Published as ASXL3(NM_030632.2):c.3106C>T (p.R1036*), ASXL3(NM_030632.3):c.3106C>T (p.(Arg1036Ter))
ISCN -
DB-ID ASXL3_000028 See all 3 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASXL3 NM_030632.1 +/. - c.3106C>T r.(?) p.(Arg1036Ter)


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