Variant #0000536302 (NC_000009.11:g.130425623G>A, NM_003165.3:c.569G>A (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.130425623G>A
DNA change (hg38) g.127663344G>A
Published as STXBP1(NM_003165.3):c.569G>A (p.(Arg190Gln)), STXBP1(NM_003165.6):c.569G>A (p.R190Q)
ISCN -
DB-ID STXBP1_000068 See all 5 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.569G>A r.(?) p.(Arg190Gln)
STXBP1 NM_003165.3 +/. - c.569G>A r.(?) p.(Arg190Gln)


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