Variant #0000564668 (NC_000018.9:g.31319409_31319410insA, NM_030632.1:c.2041_2042insA (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.31319409_31319410insA
DNA change (hg38) g.33739445_33739446insA
Published as ASXL3(NM_030632.3):c.2041_2042insA (p.S681Yfs*8)
ISCN -
DB-ID ASXL3_000025
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASXL3 NM_030632.1 +/. - c.2041_2042insA r.(?) p.(Ser681TyrfsTer8)


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