Variant #0000568860 (NC_000019.9:g.7703982C>T, NM_006949.2:c.165C>T (STXBP2))

Chromosome 19
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.7703982C>T
DNA change (hg38) g.7639096C>T
Published as STXBP2(NM_001272034.1):c.165C>T (p.I55=), STXBP2(NM_001272034.2):c.165C>T (p.I55=)
ISCN -
DB-ID PET100_000008 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) 0.00197 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
PET100 NM_001171155.1 -/. - c.*7540C>T r.(=) p.(=)
STXBP2 NM_006949.2 -/. - c.165C>T r.(?) p.(Ile55=)


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