Variant #0000990509 (NC_000001.10:g.16259376_16259377del, NM_015001.2:c.6641_6642del (SPEN))

Chromosome 1
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.16259376_16259377del
DNA change (hg38) -
Published as SPEN(NM_015001.3):c.6641_6642delAG (p.E2214Afs*11)
ISCN -
DB-ID SPEN_000054
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPEN NM_015001.2 +/. - c.6641_6642del r.(?) p.(Glu2214Alafs*11)


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