Variant #0000331333 (NC_000006.11:g.159084392_159084393del, NM_001009991.3:c.92_93del (SYTL3))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.159084392_159084393del
DNA change (hg38) g.158663360_158663361del
Published as SYTL3(NM_001242384.1):c.89_90del (p.(Thr31ArgfsTer91))
ISCN -
DB-ID SYTL3_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYTL3 NM_001009991.3 ?/. - c.92_93del r.(?) p.(Thr31ArgfsTer91)


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