Variant #0000313205 (NC_000009.11:g.130428502T>C, NM_003165.3:c.721T>C (STXBP1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.130428502T>C
DNA change (hg38) g.127666223T>C
Published as STXBP1(NM_003165.6):c.721T>C (p.S241P)
ISCN -
DB-ID STXBP1_000072
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STXBP1 NM_001032221.3 +?/. - c.721T>C r.(?) p.(Ser241Pro)
STXBP1 NM_003165.3 +?/. - c.721T>C r.(?) p.(Ser241Pro)


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