Variant #0000861395 (NC_000009.11:g.130415941C>T, NC_000009.11(NM_003165.3):c.88-53C>T (STXBP1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130415941C>T
DNA change (hg38) -
Published as STXBP1(NM_001374308.2):c.46-53C>T
ISCN -
DB-ID STXBP1_000151
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.88-53C>T r.(=) p.(=)
STXBP1 NM_003165.3 -/. - c.88-53C>T r.(=) p.(=)


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