Variant #0000915330 (NC_000019.9:g.7710082G>C, NC_000019.9(NM_006949.2):c.1247-1G>C (STXBP2))

Chromosome 19
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.7710082G>C
DNA change (hg38) -
Published as STXBP2(NM_001272034.1):c.1280-1G>C, STXBP2(NM_001272034.2):c.1280-1G>C, STXBP2(NM_006949.2):c.1247-1G>C, STXBP2(NM_006949.4):c.1247-1G>C
ISCN -
DB-ID STXBP2_000021 See all 7 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) 0.00019 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STXBP2 NM_006949.2 +/. - c.1247-1G>C r.spl? p.?


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