Variant #0000536305 (NC_000009.11:g.130435459G>T, NC_000009.11(NM_003165.3):c.1030-1G>T (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.130435459G>T
DNA change (hg38) g.127673180G>T
Published as STXBP1(NM_003165.6):c.1030-1G>T
ISCN -
DB-ID STXBP1_000117
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     
STXBP1 NM_001032221.3 +/. - c.1030-1G>T r.spl? p.?
STXBP1 NM_003165.3 +/. - c.1030-1G>T r.spl? p.?


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