Variant #0000314196 (NC_000009.11:g.130444674_130444677del, NC_000009.11(NM_003165.3):c.1548-11_1548-8del (STXBP1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130444674_130444677del
DNA change (hg38) g.127682395_127682398del
Published as STXBP1(NM_001032221.6):c.1548-11_1548-8del, STXBP1(NM_003165.6):c.1548-11_1548-8delCTCT
ISCN -
DB-ID STXBP1_000085 See all 2 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2026-01-20 18:57:21 +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.1548-11_1548-8del r.(=) p.(=)
STXBP1 NM_003165.3 -?/. - c.1548-11_1548-8del r.(=) p.(=)


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