Variant #0000861396 (NC_000009.11:g.130423440del, NM_003165.3:c.385del (STXBP1))

Chromosome 9
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.130423440del
DNA change (hg38) -
Published as STXBP1(NM_003165.3):c.385delA (p.T129Lfs*2)
ISCN -
DB-ID STXBP1_000152
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     
STXBP1 NM_001032221.3 +/. - c.385del r.(?) p.(Thr129Leufs*2)
STXBP1 NM_003165.3 +/. - c.385del r.(?) p.(Thr129Leufs*2)


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