Variant #0000527375 (NC_000006.11:g.144508133_144508134del, NM_003764.3:c.369_370del (STX11))

Chromosome 6
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.144508133_144508134del
DNA change (hg38) g.144186996_144186997del
Published as STX11(NM_003764.3):c.369_370delAG (p.V124Gfs*61)
ISCN -
DB-ID STX11_000006
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_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 2020-06-22 10:47:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STX11 NM_003764.3 +/. - c.369_370del r.(?) p.(Val124GlyfsTer61)


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