Variant #0000895258 (NC_000020.10:g.31021601_31021610del, NM_015338.5:c.1600_1609del (ASXL1))

Chromosome 20
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.31021601_31021610del
DNA change (hg38) -
Published as ASXL1(NM_015338.5):c.1600_1609delTCCTTTCCCG (p.S534Kfs*166)
ISCN -
DB-ID ASXL1_000116
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +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     
ASXL1 NM_015338.5 +/. - c.1600_1609del r.(?) p.(Ser534Lysfs*166)


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